HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17054045C>A , CM000663.2:g.17054045C>A | GRCh38 |
NC_000001.10:g.17380540C>A , CM000663.1:g.17380540C>A | GRCh37 |
NC_000001.9:g.17253127C>A | NCBI36 |
NG_012340.1:g.5126G>T , LRG_316:g.5126G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375499.7:c.-26G>T | ENSP00000364649.3:n.-26G>T | |
NM_003000.2:c.-26G>T , LRG_316t1:c.-26G>T | NP_002991.2:n.-26G>T |