Linked Data
ClinVar Variation Id:
2885454
ClinVar RCV Id:
RCV003610751
dbSNP Id:
rs763436491
ExAC:
9:140671290 C / T
gnomAD v2:
9-140671290-C-T
gnomAD v3:
9-137776838-C-T
gnomAD v4:
9-137776838-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137776838C>T , CM000671.2:g.137776838C>T | GRCh38 |
| NC_000009.11:g.140671290C>T , CM000671.1:g.140671290C>T | GRCh37 |
| NC_000009.10:g.139791111C>T | NCBI36 |
| NG_011776.1:g.162847C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000460843.6:c.2012C>T MANE Select | ENSP00000417980.1:p.Thr671Met | |
| ENST00000636027.1:c.1898C>T | ENSP00000489961.1:p.Thr633Met | |
| ENST00000637161.1:c.1919C>T | ENSP00000490328.1:p.Thr640Met | |
| ENST00000637261.1:c.2052C>T | ENSP00000490815.1:n.2052C>T | |
| ENST00000638071.1:c.1639C>T | ||
| ENST00000640639.1:c.1181C>T | ENSP00000491823.1:p.Thr394Met | |
| ENST00000371394.6:c.*1747C>T | ENSP00000485945.1:n.*1747C>T | |
| ENST00000460843.5:c.2012C>T | ENSP00000417980.1:p.Thr671Met | |
| ENST00000462484.5:c.2012C>T | ENSP00000417328.1:p.Thr671Met | |
| ENST00000462942.3:c.869C>T | ENSP00000436107.1:p.Thr290Met | |
| ENST00000626603.1:n.1611G>A | ||
| NM_001145527.1:c.2012C>T | NP_001138999.1:p.Thr671Met | |
| NM_024757.4:c.2012C>T | NP_079033.4:p.Thr671Met | |
| XM_005266105.3:c.2003C>T | XP_005266162.1:p.Thr668Met | |
| XM_005266110.1:c.1919C>T | XP_005266167.1:p.Thr640Met | |
| XM_006717288.2:c.1994C>T | XP_006717351.1:p.Thr665Met | |
| XM_011519021.1:c.2021C>T | XP_011517323.1:p.Thr674Met | |
| XM_011519022.1:c.2018C>T | XP_011517324.1:p.Thr673Met | |
| XM_011519023.1:c.2000C>T | XP_011517325.1:p.Thr667Met | |
| XM_011519024.1:c.1943C>T | XP_011517326.1:p.Thr648Met | |
| XM_011519025.1:c.1919C>T | XP_011517327.1:p.Thr640Met | |
| XM_011519026.1:c.1877C>T | XP_011517328.1:p.Thr626Met | |
| XM_011519027.1:c.2021C>T | XP_011517329.1:p.Thr674Met | |
| XM_011519028.1:c.2021C>T | XP_011517330.1:p.Thr674Met | |
| XM_011519029.1:c.443C>T | XP_011517331.1:p.Thr148Met | |
| XM_011519033.1:c.1856C>T | XP_011517335.1:p.Thr619Met | |
| NM_001354259.1:c.1919C>T | NP_001341188.1:p.Thr640Met | |
| NM_001354263.1:c.1991C>T | NP_001341192.1:p.Thr664Met | |
| XM_005266105.5:c.2003C>T | XP_005266162.1:p.Thr668Met | |
| XM_011519021.3:c.2021C>T | XP_011517323.1:p.Thr674Met | |
| XM_011519022.3:c.2018C>T | XP_011517324.1:p.Thr673Met | |
| XM_011519023.3:c.2000C>T | XP_011517325.1:p.Thr667Met | |
| XM_011519029.3:c.443C>T | XP_011517331.1:p.Thr148Met | |
| XM_017015134.1:c.1997C>T | XP_016870623.1:p.Thr666Met | |
| XM_017015136.2:c.1913C>T | XP_016870625.1:p.Thr638Met | |
| XM_017015137.1:c.1898C>T | XP_016870626.1:p.Thr633Met | |
| XM_017015138.1:c.1898C>T | XP_016870627.1:p.Thr633Met | |
| XM_024447674.1:c.1841C>T | XP_024303442.1:p.Thr614Met | |
| XM_024447675.1:c.1775C>T | XP_024303443.1:p.Thr592Met | |
| XM_024447676.1:c.1136C>T | XP_024303444.1:p.Thr379Met | |
| XM_024447677.1:c.1136C>T | XP_024303445.1:p.Thr379Met | |
| XM_024447678.1:c.1919C>T | XP_024303446.1:p.Thr640Met | |
| XM_024447679.1:c.1919C>T | XP_024303447.1:p.Thr640Met | |
| XM_024447680.1:c.1754C>T | XP_024303448.1:p.Thr585Met | |
| NM_024757.5:c.2012C>T MANE Select | NP_079033.4:p.Thr671Met | |
| NM_001145527.2:c.2012C>T | NP_001138999.1:p.Thr671Met | |
| NM_001354259.2:c.1919C>T | NP_001341188.1:p.Thr640Met | |
| NM_001354263.2:c.1991C>T | NP_001341192.1:p.Thr664Met |