HGVS | Genome Assembly |
---|---|
NC_000003.12:g.13148884C>T , CM000665.2:g.13148884C>T | GRCh38 |
NC_000003.11:g.13190384C>T , CM000665.1:g.13190384C>T | GRCh37 |
NC_000003.10:g.13165384C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648114.1:c.302+15220G>A | ENSP00000497029.1:n.302+15220G>A | |
XM_011534304.1:c.302+15220G>A | XP_011532606.1:n.302+15220G>A | |
XM_011534309.1:c.41+15122G>A | XP_011532611.1:n.41+15122G>A | |
XM_011534310.1:c.302+15220G>A | XP_011532612.1:n.302+15220G>A | |
NM_001376938.2:c.302+15220G>A | NP_001363867.1:n.302+15220G>A |