HGVS | Genome Assembly |
---|---|
NC_000014.9:g.74493511C>A , CM000676.2:g.74493511C>A | GRCh38 |
NC_000014.8:g.74960214C>A , CM000676.1:g.74960214C>A | GRCh37 |
NC_000014.7:g.74029967C>A | NCBI36 |
NG_007117.1:g.4871G>T | |
NG_033074.1:g.4792C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555592.1:c.-64+59G>T | ENSP00000450887.1:n.-64+59G>T | |
ENST00000555619.5:c.-237G>T | ENSP00000451112.1:n.-237G>T | |
ENST00000556009.5:c.147+520G>T | ||
NM_001363688.1:c.-237G>T | NP_001350617.1:n.-237G>T | |
NM_006432.4:c.-237G>T | NP_006423.1:n.-237G>T |