Linked Data
MyVariant Identifiers:
chr7:g.19156492C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19116869C>T , CM000669.2:g.19116869C>T | GRCh38 |
| NC_000007.13:g.19156492C>T , CM000669.1:g.19156492C>T | GRCh37 |
| NC_000007.12:g.19123017C>T | NCBI36 |
| NG_008114.1:g.5804G>A | |
| NG_008114.2:g.5804G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000242261.6:c.453G>A MANE Select | ENSP00000242261.5:p.Leu151= | |
| ENST00000242261.5:c.453G>A | ENSP00000242261.5:p.Leu151= | |
| ENST00000354571.5:c.250G>A | ||
| ENST00000443687.5:c.56G>A | ||
| NM_000474.3:c.453G>A | NP_000465.1:p.Leu151= | |
| XM_011515496.1:c.453G>A | XP_011513798.1:p.Leu151= | |
| NR_149001.1:n.804G>A | ||
| NM_000474.4:c.453G>A MANE Select | NP_000465.1:p.Leu151= | |
| NR_149001.2:n.768G>A |