Linked Data
MyVariant Identifiers:
chr19:g.46307570C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45804312C>T , CM000681.2:g.45804312C>T | GRCh38 |
| NC_000019.9:g.46307570C>T , CM000681.1:g.46307570C>T | GRCh37 |
| NC_000019.8:g.50999410C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221538.8:c.1593G>A MANE Select | ENSP00000221538.2:p.Val531= | |
| ENST00000221538.7:c.1593G>A | ENSP00000221538.2:p.Val531= | |
| ENST00000597055.1:c.1593G>A | ENSP00000472630.1:p.Val531= | |
| ENST00000600188.5:c.801G>A | ENSP00000471559.1:p.Val267= | |
| NM_030785.3:c.1593G>A | NP_110412.1:p.Val531= | |
| XM_011527351.1:c.1593G>A | XP_011525653.1:p.Val531= | |
| XM_011527351.2:c.1593G>A | XP_011525653.1:p.Val531= | |
| NM_030785.4:c.1593G>A MANE Select | NP_110412.1:p.Val531= |