HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8732072C>G , CM000685.2:g.8732072C>G | GRCh38 |
NC_000023.10:g.8700113C>G , CM000685.1:g.8700113C>G | GRCh37 |
NC_000023.9:g.8660113C>G | NCBI36 |
NG_007088.1:g.5115G>C | |
NG_007088.2:g.5115G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262648.8:c.-36G>C MANE Select | ENSP00000262648.3:n.-36G>C | |
ENST00000262648.7:c.-36G>C | ENSP00000262648.3:n.-36G>C | |
ENST00000619786.1:c.-36G>C | ENSP00000478734.1:n.-36G>C | |
NM_000216.2:c.-36G>C | NP_000207.2:n.-36G>C | |
XM_005274501.3:c.-36G>C | XP_005274558.1:n.-36G>C | |
NM_000216.3:c.-36G>C | NP_000207.2:n.-36G>C | |
XM_005274501.4:c.-36G>C | XP_005274558.1:n.-36G>C | |
NM_000216.4:c.-36G>C MANE Select | NP_000207.2:n.-36G>C |