HGVS | Genome Assembly |
---|---|
NC_000012.12:g.955239A>C , CM000674.2:g.955239A>C | GRCh38 |
NC_000012.11:g.1064405A>C , CM000674.1:g.1064405A>C | GRCh37 |
NC_000012.10:g.934666A>C | NCBI36 |
NG_017078.2:g.39803T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000430095.6:c.-18-22163T>G | ENSP00000387901.2:n.-18-22163T>G | |
NM_001297419.1:c.-18-22163T>G | NP_001284348.1:n.-18-22163T>G | |
XM_005253720.3:c.-18-22163T>G | XP_005253777.1:n.-18-22163T>G | |
XM_005253720.5:c.-18-22163T>G | XP_005253777.1:n.-18-22163T>G | |
XM_017019769.1:c.-18-22163T>G | XP_016875258.1:n.-18-22163T>G |