HGVS | Genome Assembly |
---|---|
NC_000007.14:g.155812196G>A , CM000669.2:g.155812196G>A | GRCh38 |
NC_000007.13:g.155604890G>A , CM000669.1:g.155604890G>A | GRCh37 |
NC_000007.12:g.155297651G>A | NCBI36 |
NG_007504.2:g.5078C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297261.7:c.-74C>T MANE Select | ENSP00000297261.2:n.-74C>T | |
ENST00000297261.6:c.-74C>T | ENSP00000297261.2:n.-74C>T | |
NM_000193.2:c.-74C>T | NP_000184.1:n.-74C>T | |
NM_000193.3:c.-74C>T | NP_000184.1:n.-74C>T | |
NM_000193.4:c.-74C>T MANE Select | NP_000184.1:n.-74C>T |