HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117325T>A , CM000669.2:g.19117325T>A | GRCh38 |
NC_000007.13:g.19156948T>A , CM000669.1:g.19156948T>A | GRCh37 |
NC_000007.12:g.19123473T>A | NCBI36 |
NG_008114.1:g.5348A>T | |
NG_008114.2:g.5348A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.-4A>T MANE Select | ENSP00000242261.5:n.-4A>T | |
ENST00000242261.5:c.-4A>T | ENSP00000242261.5:n.-4A>T | |
NM_000474.3:c.-4A>T | NP_000465.1:n.-4A>T | |
XM_011515496.1:c.-4A>T | XP_011513798.1:n.-4A>T | |
NR_149001.1:n.348A>T | ||
NM_000474.4:c.-4A>T MANE Select | NP_000465.1:n.-4A>T | |
NR_149001.2:n.312A>T |