HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31658212C>T , CM000668.2:g.31658212C>T | GRCh38 |
NC_000006.11:g.31625989C>T , CM000668.1:g.31625989C>T | GRCh37 |
NC_000006.10:g.31733968C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XM_011514895.1:c.-14+2109G>A | XP_011513197.1:n.-14+2109G>A | |
XM_017011279.2:c.-14+2109G>A | XP_016866768.1:n.-14+2109G>A |