HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81577901C>T , CM000665.2:g.81577901C>T | GRCh38 |
NC_000003.11:g.81627052C>T , CM000665.1:g.81627052C>T | GRCh37 |
NC_000003.10:g.81709742C>T | NCBI36 |
NG_011810.1:g.188900G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.1618+24G>A MANE Select | ENSP00000410833.2:n.1618+24G>A | |
ENST00000429644.6:c.1618+24G>A | ENSP00000410833.2:n.1618+24G>A | |
ENST00000484687.1:n.19+24G>A | ||
ENST00000489715.1:c.1495+24G>A | ENSP00000419638.1:n.1495+24G>A | |
NM_000158.3:c.1618+24G>A | NP_000149.3:n.1618+24G>A | |
NM_000158.4:c.1618+24G>A MANE Select | NP_000149.4:n.1618+24G>A |