Linked Data
MyVariant Identifiers:
chr16:g.89245895T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89179487T>A , CM000678.2:g.89179487T>A | GRCh38 |
| NC_000016.9:g.89245895T>A , CM000678.1:g.89245895T>A | GRCh37 |
| NC_000016.8:g.87773396T>A | NCBI36 |
| NG_012055.1:g.12733T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289746.3:c.114T>A MANE Select | ENSP00000289746.2:p.Pro38= | |
| ENST00000289746.2:c.114T>A | ENSP00000289746.2:p.Pro38= | |
| ENST00000521087.5:n.179T>A | ||
| ENST00000524089.1:n.179T>A | ||
| NM_004933.2:c.114T>A | NP_004924.1:p.Pro38= | |
| XM_011522806.1:c.114T>A | XP_011521108.1:p.Pro38= | |
| NM_004933.3:c.114T>A MANE Select | NP_004924.1:p.Pro38= |