Linked Data
dbSNP Id:
rs1841454546
gnomAD v4:
10-80274525-A-G
MyVariant Identifiers:
chr10:g.82034281A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80274525A>G , CM000672.2:g.80274525A>G | GRCh38 |
| NC_000010.10:g.82034281A>G , CM000672.1:g.82034281A>G | GRCh37 |
| NC_000010.9:g.82024261A>G | NCBI36 |
| NG_008083.1:g.20154T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.1080T>C MANE Select | ENSP00000361287.3:p.Ile360= | |
| ENST00000372213.7:c.1080T>C | ENSP00000361287.3:p.Ile360= | |
| ENST00000480845.1:n.312T>C | ||
| ENST00000485270.5:n.592T>C | ||
| NM_000429.2:c.1080T>C | NP_000420.1:p.Ile360= | |
| XM_005269842.3:c.1080T>C | XP_005269899.1:p.Ile360= | |
| XM_005269843.3:c.957T>C | XP_005269900.1:p.Ile319= | |
| NM_000429.3:c.1080T>C MANE Select | NP_000420.1:p.Ile360= |