HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31658231C>T , CM000668.2:g.31658231C>T | GRCh38 |
NC_000006.11:g.31626008C>T , CM000668.1:g.31626008C>T | GRCh37 |
NC_000006.10:g.31733987C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XM_011514895.1:c.-14+2090G>A | XP_011513197.1:n.-14+2090G>A | |
XM_017011279.2:c.-14+2090G>A | XP_016866768.1:n.-14+2090G>A |