Linked Data
MyVariant Identifiers:
chr1:g.24194483C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.23867993C>T , CM000663.2:g.23867993C>T | GRCh38 |
| NC_000001.10:g.24194483C>T , CM000663.1:g.24194483C>T | GRCh37 |
| NC_000001.9:g.24067070C>T | NCBI36 |
| NG_013346.1:g.5377G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374479.4:c.294G>A MANE Select | ENSP00000363603.3:p.Pro98= | |
| ENST00000374479.3:c.294G>A | ENSP00000363603.3:p.Pro98= | |
| NM_000147.4:c.294G>A | NP_000138.2:p.Pro98= | |
| XM_005245821.1:c.-256G>A | XP_005245878.1:n.-256G>A | |
| XM_005245821.3:c.-256G>A | XP_005245878.1:n.-256G>A | |
| NM_000147.5:c.294G>A MANE Select | NP_000138.2:p.Pro98= | |
| NR_174379.1:n.298G>A | ||
| NR_174380.1:n.298G>A | ||
| NR_174381.1:n.298G>A | ||
| NR_174382.1:n.298G>A |