HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20756777G>A , CM000686.2:g.20756777G>A | GRCh38 |
NC_000024.9:g.22918663G>A , CM000686.1:g.22918663G>A | GRCh37 |
NC_000024.8:g.21328051G>A | NCBI36 |
NG_032924.1:g.5710G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000629237.2:c.4-1G>A MANE Select | ENSP00000486252.1:n.4-1G>A | |
ENST00000629237.1:c.4-1G>A | ENSP00000486252.1:n.4-1G>A | |
NM_001039567.2:c.4-1G>A | NP_001034656.1:n.4-1G>A | |
NM_001039567.3:c.4-1G>A MANE Select | NP_001034656.1:n.4-1G>A |