HGVS | Genome Assembly |
---|---|
NC_000014.9:g.93218654G>T , CM000676.2:g.93218654G>T | GRCh38 |
NC_000014.8:g.93685000G>T , CM000676.1:g.93685000G>T | GRCh37 |
NC_000014.7:g.92754753G>T | NCBI36 |
NG_051089.1:g.16599G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000013070.11:c.729G>T MANE Select | ENSP00000013070.6:p.Gln243His | |
ENST00000013070.10:c.729G>T | ENSP00000013070.6:p.Gln243His | |
ENST00000416753.5:c.501G>T | ENSP00000391706.2:p.Gln167His | |
ENST00000553674.1:c.*430G>T | ENSP00000450470.1:n.*430G>T | |
ENST00000553857.5:c.378+3373G>T | ||
ENST00000556871.5:c.438G>T | ENSP00000451022.1:p.Gln146His | |
NM_175748.3:c.729G>T | NP_786924.2:p.Gln243His | |
NR_038150.1:n.831G>T | ||
NM_175748.4:c.729G>T MANE Select | NP_786924.2:p.Gln243His | |
NR_038150.2:n.631G>T |