Linked Data
MyVariant Identifiers:
chr1:g.17672556G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17346061G>C , CM000663.2:g.17346061G>C | GRCh38 |
| NC_000001.10:g.17672556G>C , CM000663.1:g.17672556G>C | GRCh37 |
| NC_000001.9:g.17545143G>C | NCBI36 |
| NG_023261.2:g.42872G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375448.4:c.969G>C MANE Select | ENSP00000364597.4:p.Val323= | |
| ENST00000468945.1:n.28G>C | ||
| NM_012387.2:c.969G>C | NP_036519.2:p.Val323= | |
| XM_011541150.1:c.783G>C | XP_011539452.1:p.Val261= | |
| XM_011541151.1:c.969G>C | XP_011539453.1:p.Val323= | |
| XM_011541152.1:c.432G>C | XP_011539454.1:p.Val144= | |
| XM_011541153.1:c.969G>C | XP_011539455.1:p.Val323= | |
| XM_011541154.1:c.969G>C | XP_011539456.1:p.Val323= | |
| XM_011541155.1:c.969G>C | XP_011539457.1:p.Val323= | |
| XM_011541156.1:c.969G>C | XP_011539458.1:p.Val323= | |
| XM_011541157.1:c.78G>C | XP_011539459.1:p.Val26= | |
| XM_011541154.2:c.969G>C | XP_011539456.1:p.Val323= | |
| NM_012387.3:c.969G>C MANE Select | NP_036519.2:p.Val323= |