Linked Data
MyVariant Identifiers:
chr1:g.15772145G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15445650G>T , CM000663.2:g.15445650G>T | GRCh38 |
| NC_000001.10:g.15772145G>T , CM000663.1:g.15772145G>T | GRCh37 |
| NC_000001.9:g.15644732G>T | NCBI36 |
| NG_009253.1:g.12208G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.693G>T MANE Select | ENSP00000365116.4:p.Val231= | |
| ENST00000375943.6:c.*147G>T | ENSP00000365110.2:n.*147G>T | |
| ENST00000375949.4:c.693G>T | ENSP00000365116.4:p.Val231= | |
| ENST00000483406.1:n.457G>T | ||
| NM_007272.2:c.693G>T | NP_009203.2:p.Val231= | |
| XM_011540550.1:c.547G>T | XP_011538852.1:p.Val183Phe | |
| NM_007272.3:c.693G>T MANE Select | NP_009203.2:p.Val231= |