HGVS | Genome Assembly |
---|---|
NC_000002.12:g.31580974G>C , CM000664.2:g.31580974G>C | GRCh38 |
NC_000002.11:g.31806043G>C , CM000664.1:g.31806043G>C | GRCh37 |
NC_000002.10:g.31659547G>C | NCBI36 |
NG_008365.1:g.4998C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000622030.1:c.-74C>G | ENSP00000477587.1:n.-74C>G | |
XM_011533068.1:c.-74C>G | XP_011531370.1:n.-74C>G | |
XM_011533070.1:c.27-47208C>G | XP_011531372.1:n.27-47208C>G | |
XM_011533071.1:c.27-47208C>G | XP_011531373.1:n.27-47208C>G | |
XM_011533072.1:c.27-47208C>G | XP_011531374.1:n.27-47208C>G | |
XM_011533072.2:c.27-47208C>G | XP_011531374.1:n.27-47208C>G |