HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42184483G>A , CM000679.2:g.42184483G>A | GRCh38 |
NC_000017.10:g.40336501G>A , CM000679.1:g.40336501G>A | GRCh37 |
NC_000017.9:g.37590027G>A | NCBI36 |
NG_011448.1:g.5970C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293330.1:c.67C>T MANE Select | ENSP00000293330.1:p.Pro23Ser | |
NM_001524.1:c.67C>T MANE Select | NP_001515.1:p.Pro23Ser |