Linked Data
ClinVar Variation Id:
365188
ClinVar RCV Id:
RCV001548234
dbSNP Id:
rs11543348
gnomAD v2:
9-131395768-G-A
gnomAD v3:
9-128633489-G-A
gnomAD v4:
9-128633489-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.128633489G>A , CM000671.2:g.128633489G>A | GRCh38 |
| NC_000009.11:g.131395768G>A , CM000671.1:g.131395768G>A | GRCh37 |
| NC_000009.10:g.130435589G>A | NCBI36 |
| NG_027748.1:g.85932G>A | |
| NG_034056.1:g.28362C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000627441.3:c.*155G>A | ENSP00000486547.2:n.*155G>A | |
| ENST00000704202.1:c.*155G>A | ENSP00000515764.1:n.*155G>A | |
| ENST00000704203.1:c.*155G>A | ENSP00000515765.1:n.*155G>A | |
| ENST00000704204.1:c.7115G>A | ENSP00000515766.1:n.7115G>A | |
| ENST00000704206.1:c.5194G>A | ||
| ENST00000706487.1:c.*155G>A | ENSP00000516412.1:n.*155G>A | |
| ENST00000372739.7:c.*155G>A MANE Select | ENSP00000361824.4:n.*155G>A | |
| ENST00000636010.1:n.1313G>A | ||
| ENST00000358161.9:c.*155G>A | ENSP00000350882.6:n.*155G>A | |
| ENST00000372731.8:c.*155G>A | ENSP00000361816.4:n.*155G>A | |
| ENST00000372739.5:c.*155G>A | ENSP00000361824.3:n.*155G>A | |
| ENST00000625980.2:n.1543G>A | ||
| ENST00000630147.1:n.612G>A | ||
| ENST00000630763.1:n.1346G>A | ||
| ENST00000630804.2:c.*155G>A | ENSP00000486308.1:n.*155G>A | |
| NM_001130438.2:c.*155G>A | NP_001123910.1:n.*155G>A | |
| NM_001195532.1:c.*155G>A | NP_001182461.1:n.*155G>A | |
| NM_003127.3:c.*155G>A | NP_003118.2:n.*155G>A | |
| XM_006717245.1:c.*155G>A | XP_006717308.1:n.*155G>A | |
| XM_006717246.1:c.*155G>A | XP_006717309.1:n.*155G>A | |
| XM_006717247.1:c.*155G>A | XP_006717310.1:n.*155G>A | |
| XM_006717248.1:c.*155G>A | XP_006717311.1:n.*155G>A | |
| XM_006717249.1:c.*155G>A | XP_006717312.1:n.*155G>A | |
| XM_006717250.1:c.*155G>A | XP_006717313.1:n.*155G>A | |
| XM_006717251.1:c.*155G>A | XP_006717314.1:n.*155G>A | |
| XM_006717252.1:c.*155G>A | XP_006717315.1:n.*155G>A | |
| XM_006717253.1:c.*155G>A | XP_006717316.1:n.*155G>A | |
| XM_006717254.1:c.*155G>A | XP_006717317.1:n.*155G>A | |
| NM_001363759.1:c.*155G>A | NP_001350688.1:n.*155G>A | |
| NM_001363765.1:c.*155G>A | NP_001350694.1:n.*155G>A | |
| XM_006717247.2:c.*155G>A | XP_006717310.1:n.*155G>A | |
| XM_006717248.2:c.*155G>A | XP_006717311.1:n.*155G>A | |
| XM_006717251.2:c.*155G>A | XP_006717314.1:n.*155G>A | |
| XM_006717252.3:c.*155G>A | XP_006717315.1:n.*155G>A | |
| XM_017015059.1:c.*155G>A | XP_016870548.1:n.*155G>A | |
| XM_017015060.1:c.*155G>A | XP_016870549.1:n.*155G>A | |
| NM_001130438.3:c.*155G>A MANE Select | NP_001123910.1:n.*155G>A | |
| NM_001195532.2:c.*155G>A | NP_001182461.1:n.*155G>A | |
| NM_001363759.2:c.*155G>A | NP_001350688.1:n.*155G>A | |
| NM_001363765.2:c.*155G>A | NP_001350694.1:n.*155G>A | |
| NM_001375310.1:c.*155G>A | NP_001362239.1:n.*155G>A | |
| NM_001375311.2:c.*155G>A | NP_001362240.1:n.*155G>A | |
| NM_001375312.2:c.*155G>A | NP_001362241.2:n.*155G>A | |
| NM_001375313.1:c.*155G>A | NP_001362242.1:n.*155G>A | |
| NM_001375314.2:c.*155G>A | NP_001362243.1:n.*155G>A | |
| NM_001375318.1:c.*155G>A | NP_001362247.1:n.*155G>A | |
| NM_003127.4:c.*155G>A | NP_003118.2:n.*155G>A |