HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31658216T>C , CM000668.2:g.31658216T>C | GRCh38 |
NC_000006.11:g.31625993T>C , CM000668.1:g.31625993T>C | GRCh37 |
NC_000006.10:g.31733972T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011514895.1:c.-14+2105A>G | XP_011513197.1:n.-14+2105A>G | |
XM_017011279.2:c.-14+2105A>G | XP_016866768.1:n.-14+2105A>G |