Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562967G>T , CM000682.2:g.57562967G>T | GRCh38 |
| NC_000020.10:g.56138023G>T , CM000682.1:g.56138023G>T | GRCh37 |
| NC_000020.9:g.55571429G>T | NCBI36 |
| NG_008205.1:g.6887G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.611-61G>T MANE Select | ENSP00000319814.4:n.611-61G>T | |
| ENST00000319441.5:c.611-61G>T | ENSP00000319814.4:n.611-61G>T | |
| ENST00000467047.1:n.1888G>T | ||
| ENST00000470051.1:n.134G>T | ||
| ENST00000498194.1:n.553-61G>T | ||
| NM_002591.3:c.611-61G>T | NP_002582.3:n.611-61G>T | |
| XM_011528839.1:c.215-61G>T | XP_011527141.1:n.215-61G>T | |
| XM_024451888.1:c.215-61G>T | XP_024307656.1:n.215-61G>T | |
| NM_002591.4:c.611-61G>T MANE Select | NP_002582.3:n.611-61G>T |