HGVS | Genome Assembly |
---|---|
NC_000005.10:g.174724586C>A , CM000667.2:g.174724586C>A | GRCh38 |
NC_000005.9:g.174151589C>A , CM000667.1:g.174151589C>A | GRCh37 |
NC_000005.8:g.174084195C>A | NCBI36 |
NG_008124.1:g.5015C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239243.7:c.-74C>A MANE Select | ENSP00000239243.5:n.-74C>A | |
ENST00000239243.6:c.-74C>A | ENSP00000239243.5:n.-74C>A | |
NM_002449.4:c.-74C>A | NP_002440.2:n.-74C>A | |
NM_001363626.1:c.-74C>A | NP_001350555.1:n.-74C>A | |
NM_002449.5:c.-74C>A MANE Select | NP_002440.2:n.-74C>A | |
NM_001363626.2:c.-74C>A | NP_001350555.1:n.-74C>A |