HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218893290G>T , CM000664.2:g.218893290G>T | GRCh38 |
NC_000002.11:g.219758012G>T , CM000664.1:g.219758012G>T | GRCh37 |
NC_000002.10:g.219466256G>T | NCBI36 |
NG_012179.1:g.17758G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258411.8:c.*19G>T MANE Select | ENSP00000258411.3:n.*19G>T | |
ENST00000258411.7:c.*19G>T | ENSP00000258411.3:n.*19G>T | |
ENST00000489887.1:n.47+23G>T | ||
NM_025216.2:c.*19G>T | NP_079492.2:n.*19G>T | |
XM_011511928.1:c.*19G>T | XP_011510230.1:n.*19G>T | |
XM_011511929.1:c.*19G>T | XP_011510231.1:n.*19G>T | |
XM_011511930.1:c.893G>T | XP_011510232.1:p.Gly298Val | |
XM_011511929.2:c.*19G>T | XP_011510231.1:n.*19G>T | |
NM_025216.3:c.*19G>T MANE Select | NP_079492.2:n.*19G>T |