HGVS | Genome Assembly |
---|---|
NC_000009.12:g.119339287G>A , CM000671.2:g.119339287G>A | GRCh38 |
NC_000009.11:g.122101565G>A , CM000671.1:g.122101565G>A | GRCh37 |
NC_000009.10:g.121141386G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000265922.8:c.-50-25882C>T MANE Select | ENSP00000265922.2:n.-50-25882C>T | |
ENST00000265922.7:c.-50-25882C>T | ENSP00000265922.2:n.-50-25882C>T | |
ENST00000373964.2:c.-50-25882C>T | ENSP00000363075.1:n.-50-25882C>T | |
NM_014618.2:c.-50-25882C>T | NP_055433.2:n.-50-25882C>T | |
NM_014618.3:c.-50-25882C>T MANE Select | NP_055433.2:n.-50-25882C>T |