HGVS | Genome Assembly |
---|---|
NC_000019.10:g.4816165G>T , CM000681.2:g.4816165G>T | GRCh38 |
NC_000019.9:g.4816177G>T , CM000681.1:g.4816177G>T | GRCh37 |
NC_000019.8:g.4767177G>T | NCBI36 |
NG_031998.1:g.20578C>A , LRG_358:g.20578C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248244.6:c.*74C>A MANE Select | ENSP00000248244.4:n.*74C>A | |
ENST00000248244.5:c.*74C>A | ENSP00000248244.4:n.*74C>A | |
NM_182919.3:c.*74C>A , LRG_358t1:c.*74C>A | NP_891549.1:n.*74C>A | |
NM_001385678.1:c.*74C>A | NP_001372607.1:n.*74C>A | |
NM_001385679.1:c.*74C>A | NP_001372608.1:n.*74C>A | |
NM_001385680.1:c.*74C>A | NP_001372609.1:n.*74C>A | |
NM_182919.4:c.*74C>A MANE Select | NP_891549.1:n.*74C>A |