Linked Data
MyVariant Identifiers:
chr1:g.229567387G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431640G>T , CM000663.2:g.229431640G>T | GRCh38 |
| NC_000001.10:g.229567387G>T , CM000663.1:g.229567387G>T | GRCh37 |
| NC_000001.9:g.227634010G>T | NCBI36 |
| NG_006672.1:g.7457C>A , LRG_429:g.7457C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000366683.4:c.991-76C>A | ENSP00000355644.4:n.991-76C>A | |
| ENST00000684723.1:c.858C>A | ENSP00000508084.1:p.Ile286= | |
| ENST00000366683.3:c.624C>A | ENSP00000355644.3:p.Ile208= | |
| ENST00000366684.7:c.993C>A MANE Select | ENSP00000355645.3:p.Ile331= | |
| NM_001100.3:c.993C>A , LRG_429t1:c.993C>A | NP_001091.1:p.Ile331= | |
| NM_001100.4:c.993C>A MANE Select | NP_001091.1:p.Ile331= |