HGVS | Genome Assembly |
---|---|
NC_000014.9:g.74493460A>C , CM000676.2:g.74493460A>C | GRCh38 |
NC_000014.8:g.74960163A>C , CM000676.1:g.74960163A>C | GRCh37 |
NC_000014.7:g.74029916A>C | NCBI36 |
NG_007117.1:g.4922T>G | |
NG_033074.1:g.4741A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555592.1:c.-64+110T>G | ENSP00000450887.1:n.-64+110T>G | |
ENST00000555619.5:c.-186T>G | ENSP00000451112.1:n.-186T>G | |
ENST00000556009.5:c.147+571T>G | ||
NM_001363688.1:c.-186T>G | NP_001350617.1:n.-186T>G | |
NM_006432.4:c.-186T>G | NP_006423.1:n.-186T>G |