HGVS | Genome Assembly |
---|---|
NC_000014.9:g.49622069C>T , CM000676.2:g.49622069C>T | GRCh38 |
NC_000014.8:g.50088787C>T , CM000676.1:g.50088787C>T | GRCh37 |
NC_000014.7:g.49158537C>T | NCBI36 |
NG_008920.1:g.6299C>T | |
NG_033054.1:g.3563G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305386.4:c.801C>T MANE Select | ENSP00000307423.2:p.Asp267= | |
ENST00000305386.3:c.801C>T | ENSP00000307423.2:p.Asp267= | |
NM_002408.3:c.801C>T | NP_002399.1:p.Asp267= | |
NM_002408.4:c.801C>T MANE Select | NP_002399.1:p.Asp267= |