HGVS | Genome Assembly |
---|---|
NC_000002.12:g.31586832T>C , CM000664.2:g.31586832T>C | GRCh38 |
NC_000002.11:g.31811901T>C , CM000664.1:g.31811901T>C | GRCh37 |
NC_000002.10:g.31665405T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011533070.1:c.27-53066A>G | XP_011531372.1:n.27-53066A>G | |
XM_011533071.1:c.27-53066A>G | XP_011531373.1:n.27-53066A>G | |
XM_011533072.1:c.27-53066A>G | XP_011531374.1:n.27-53066A>G | |
XM_011533072.2:c.27-53066A>G | XP_011531374.1:n.27-53066A>G |