Linked Data
ClinVar Variation Id:
536303
ClinVar RCV Id:
RCV000644680
dbSNP Id:
rs935626079
gnomAD v2:
17-44115939-C-T
gnomAD v3:
17-46038573-C-T
gnomAD v4:
17-46038573-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46038573C>T , CM000679.2:g.46038573C>T | GRCh38 |
| NC_000017.10:g.44115939C>T , CM000679.1:g.44115939C>T | GRCh37 |
| NC_000017.9:g.41471786C>T | NCBI36 |
| NG_032784.1:g.191802G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432791.7:c.2506G>A MANE Select | ENSP00000387393.3:p.Ala836Thr | |
| ENST00000572904.6:c.2506G>A | ENSP00000461484.1:p.Ala836Thr | |
| ENST00000573286.2:n.4189G>A | ||
| ENST00000574590.6:c.2506G>A | ENSP00000461812.2:p.Ala836Thr | |
| ENST00000575318.6:c.2317G>A | ENSP00000461299.1:p.Ala773Thr | |
| ENST00000576137.2:n.503G>A | ||
| ENST00000638275.1:c.2317G>A | ENSP00000492576.1:p.Ala773Thr | |
| ENST00000639150.1:c.1240G>A | ENSP00000491906.1:p.Ala414Thr | |
| ENST00000639467.1:c.169G>A | ENSP00000492741.1:p.Ala57Thr | |
| ENST00000639531.1:c.2317G>A | ENSP00000491765.1:p.Ala773Thr | |
| ENST00000640636.1:c.459G>A | ||
| ENST00000648792.1:c.2506G>A | ENSP00000497628.1:p.Ala836Thr | |
| ENST00000262419.10:c.2506G>A | ENSP00000262419.6:p.Ala836Thr | |
| ENST00000432791.5:c.2506G>A | ENSP00000387393.2:p.Ala836Thr | |
| ENST00000572218.5:n.6723G>A | ||
| ENST00000572904.5:c.2506G>A | ENSP00000461484.1:p.Ala836Thr | |
| ENST00000573286.1:n.362G>A | ||
| ENST00000574590.5:c.2506G>A | ENSP00000461812.1:p.Ala836Thr | |
| ENST00000575318.5:c.2317G>A | ENSP00000461299.1:p.Ala773Thr | |
| ENST00000576137.1:n.145G>A | ||
| ENST00000576870.5:n.478G>A | ||
| NM_001193465.1:c.2506G>A | NP_001180394.1:p.Ala836Thr | |
| NM_001193466.1:c.2506G>A | NP_001180395.1:p.Ala836Thr | |
| NM_015443.3:c.2506G>A | NP_056258.1:p.Ala836Thr | |
| XM_006721823.1:c.2506G>A | XP_006721886.1:p.Ala836Thr | |
| XM_006721824.2:c.2506G>A | XP_006721887.1:p.Ala836Thr | |
| XM_011524628.1:c.2506G>A | XP_011522930.1:p.Ala836Thr | |
| XM_011524629.1:c.2404G>A | XP_011522931.1:p.Ala802Thr | |
| XM_011524630.1:c.2317G>A | XP_011522932.1:p.Ala773Thr | |
| XM_011524631.1:c.2317G>A | XP_011522933.1:p.Ala773Thr | |
| XM_011524632.1:c.1276G>A | XP_011522934.1:p.Ala426Thr | |
| XM_006721823.2:c.2506G>A | XP_006721886.1:p.Ala836Thr | |
| XM_006721824.4:c.2506G>A | XP_006721887.1:p.Ala836Thr | |
| XM_011524628.3:c.2506G>A | XP_011522930.1:p.Ala836Thr | |
| XM_011524629.3:c.2404G>A | XP_011522931.1:p.Ala802Thr | |
| XM_011524630.3:c.2317G>A | XP_011522932.1:p.Ala773Thr | |
| XM_011524631.3:c.2317G>A | XP_011522933.1:p.Ala773Thr | |
| XM_011524632.3:c.1276G>A | XP_011522934.1:p.Ala426Thr | |
| XM_017024488.2:c.2317G>A | XP_016879977.1:p.Ala773Thr | |
| XM_017024489.1:c.2404G>A | XP_016879978.1:p.Ala802Thr | |
| NM_001193466.2:c.2506G>A | NP_001180395.1:p.Ala836Thr | |
| NM_015443.4:c.2506G>A MANE Select | NP_056258.1:p.Ala836Thr | |
| NM_001193465.2:c.2506G>A | NP_001180394.1:p.Ala836Thr | |
| NM_001379198.1:c.2506G>A | NP_001366127.1:p.Ala836Thr |