Linked Data
MyVariant Identifiers:
chr7:g.19156489C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19116866C>A , CM000669.2:g.19116866C>A | GRCh38 |
| NC_000007.13:g.19156489C>A , CM000669.1:g.19156489C>A | GRCh37 |
| NC_000007.12:g.19123014C>A | NCBI36 |
| NG_008114.1:g.5807G>T | |
| NG_008114.2:g.5807G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000242261.6:c.456G>T MANE Select | ENSP00000242261.5:p.Ala152= | |
| ENST00000242261.5:c.456G>T | ENSP00000242261.5:p.Ala152= | |
| ENST00000354571.5:c.253G>T | ||
| ENST00000443687.5:c.59G>T | ||
| NM_000474.3:c.456G>T | NP_000465.1:p.Ala152= | |
| XM_011515496.1:c.456G>T | XP_011513798.1:p.Ala152= | |
| NR_149001.1:n.807G>T | ||
| NM_000474.4:c.456G>T MANE Select | NP_000465.1:p.Ala152= | |
| NR_149001.2:n.771G>T |