Linked Data
dbSNP Id:
rs11600808
ExAC:
11:68703864 C / T
gnomAD v2:
11-68703864-C-T
gnomAD v4:
11-68936396-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68936396C>T , CM000673.2:g.68936396C>T | GRCh38 |
| NC_000011.9:g.68703864C>T , CM000673.1:g.68703864C>T | GRCh37 |
| NC_000011.8:g.68460440C>T | NCBI36 |
| NG_007976.1:g.37546C>T , LRG_250:g.37546C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255078.8:c.1916C>T MANE Select | ENSP00000255078.4:p.Ala639Val | |
| ENST00000674675.1:c.160C>T | ||
| ENST00000674878.1:c.160C>T | ||
| ENST00000674955.1:c.*633C>T | ENSP00000502463.1:n.*633C>T | |
| ENST00000675118.1:c.1404C>T | ||
| ENST00000675389.1:n.191C>T | ||
| ENST00000675615.1:c.1916C>T | ENSP00000502413.1:p.Ala639Val | |
| ENST00000675648.1:n.1291C>T | ||
| ENST00000675916.1:c.160C>T | ||
| ENST00000676173.1:n.2661C>T | ||
| ENST00000676182.1:c.347C>T | ||
| ENST00000676228.1:c.*1239C>T | ENSP00000502375.1:n.*1239C>T | |
| ENST00000255078.7:c.1916C>T | ENSP00000255078.3:p.Ala639Val | |
| ENST00000539064.5:n.1675C>T | ||
| ENST00000543739.5:n.909C>T | ||
| ENST00000545475.1:n.512C>T | ||
| NM_002180.2:c.1916C>T , LRG_250t1:c.1916C>T | NP_002171.2:p.Ala639Val | |
| XM_005273974.2:c.905C>T | XP_005274031.1:p.Ala302Val | |
| XM_005273975.2:c.788C>T | XP_005274032.1:p.Ala263Val | |
| XM_011544994.1:c.683C>T | XP_011543296.1:p.Ala228Val | |
| XR_949903.1:n.2018C>T | ||
| XM_005273975.3:c.788C>T | XP_005274032.1:p.Ala263Val | |
| XM_017017669.2:c.905C>T | XP_016873158.1:p.Ala302Val | |
| XM_017017670.2:c.905C>T | XP_016873159.1:p.Ala302Val | |
| XR_949903.3:n.2014C>T | ||
| NM_002180.3:c.1916C>T MANE Select | NP_002171.2:p.Ala639Val |