HGVS | Genome Assembly |
---|---|
NC_000007.14:g.155812370C>A , CM000669.2:g.155812370C>A | GRCh38 |
NC_000007.13:g.155605064C>A , CM000669.1:g.155605064C>A | GRCh37 |
NC_000007.12:g.155297825C>A | NCBI36 |
NG_007504.2:g.4904G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297261.7:c.-248G>T MANE Select | ENSP00000297261.2:n.-248G>T | |
NM_000193.4:c.-248G>T MANE Select | NP_000184.1:n.-248G>T |