Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.120665152C>T , CM000669.2:g.120665152C>T | GRCh38 |
| NC_000007.13:g.120305206C>T , CM000669.1:g.120305206C>T | GRCh37 |
| NC_000007.12:g.120092442C>T | NCBI36 |
| NG_034230.1:g.396485C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000331113.9:c.1116-67751C>T MANE Select | ENSP00000333496.4:n.1116-67751C>T | |
| ENST00000331113.8:c.1116-67751C>T | ENSP00000333496.4:n.1116-67751C>T | |
| NM_012281.2:c.1116-67751C>T | NP_036413.1:n.1116-67751C>T | |
| NM_012281.3:c.1116-67751C>T MANE Select | NP_036413.1:n.1116-67751C>T |