Linked Data
ClinVar Variation Id:
1639705
ClinVar RCV Id:
RCV002129247
dbSNP Id:
rs2118858805
MyVariant Identifiers:
chr9:g.37424878C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.37424881C>T , CM000671.2:g.37424881C>T | GRCh38 |
| NC_000009.11:g.37424878C>T , CM000671.1:g.37424878C>T | GRCh37 |
| NC_000009.10:g.37414878C>T | NCBI36 |
| NG_008135.1:g.7172C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318158.11:c.120C>T MANE Select | ENSP00000313432.6:p.Ile40= | |
| ENST00000318158.10:c.120C>T | ENSP00000313432.6:p.Ile40= | |
| ENST00000377824.8:n.157C>T | ||
| ENST00000460882.5:n.147C>T | ||
| ENST00000487399.5:n.129C>T | ||
| ENST00000491488.5:n.109+2048C>T | ||
| ENST00000493368.5:n.177C>T | ||
| ENST00000607784.1:c.120C>T | ENSP00000475569.1:p.Ile40= | |
| NM_012203.1:c.120C>T | NP_036335.1:p.Ile40= | |
| XM_005251631.1:c.83+2048C>T | XP_005251688.1:n.83+2048C>T | |
| XM_011518073.1:c.-643C>T | XP_011516375.1:n.-643C>T | |
| XR_929374.1:n.205C>T | ||
| XM_017015320.2:c.120C>T | XP_016870809.1:p.Ile40= | |
| XM_017015321.2:c.120C>T | XP_016870810.1:p.Ile40= | |
| XM_017015323.2:c.-643C>T | XP_016870812.1:n.-643C>T | |
| XM_024447716.1:c.393C>T | XP_024303484.1:p.Ile131= | |
| XM_024447717.1:c.393C>T | XP_024303485.1:p.Ile131= | |
| XR_002956828.1:n.408C>T | ||
| XR_002956829.1:n.408C>T | ||
| XR_002956830.1:n.179C>T | ||
| XR_002956831.1:n.138+2048C>T | ||
| XR_002956832.1:n.179C>T | ||
| NM_012203.2:c.120C>T MANE Select | NP_036335.1:p.Ile40= |