HGVS | Genome Assembly |
---|---|
NC_000001.11:g.116925212G>T , CM000663.2:g.116925212G>T | GRCh38 |
NC_000001.10:g.117467834G>T , CM000663.1:g.117467834G>T | GRCh37 |
NC_000001.9:g.117269357G>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000393203.3:c.49+14960G>T MANE Select | ENSP00000376899.2:n.49+14960G>T | |
ENST00000393203.2:c.49+14960G>T | ENSP00000376899.2:n.49+14960G>T | |
NM_020440.3:c.49+14960G>T | NP_065173.2:n.49+14960G>T | |
NM_020440.4:c.49+14960G>T MANE Select | NP_065173.2:n.49+14960G>T |