HGVS | Genome Assembly |
---|---|
NC_000006.12:g.136822463T>C , CM000668.2:g.136822463T>C | GRCh38 |
NC_000006.11:g.137143601T>C , CM000668.1:g.137143601T>C | GRCh37 |
NC_000006.10:g.137185294T>C | NCBI36 |
NG_008462.1:g.4884T>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_006715502.1:c.-203T>C | XP_006715565.1:n.-203T>C | |
XM_011535900.1:c.-203T>C | XP_011534202.1:n.-203T>C | |
XM_006715502.2:c.-203T>C | XP_006715565.1:n.-203T>C | |
XM_017010934.2:c.-203T>C | XP_016866423.1:n.-203T>C |