HGVS | Genome Assembly |
---|---|
NC_000005.10:g.132556936C>G , CM000667.2:g.132556936C>G | GRCh38 |
NC_000005.9:g.131892628C>G , CM000667.1:g.131892628C>G | GRCh37 |
NC_000005.8:g.131920527C>G | NCBI36 |
NG_021151.1:g.5013C>G | |
NG_021151.2:g.4960C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000638452.2:c.-168-2348C>G | ENSP00000492349.2:n.-168-2348C>G | |
ENST00000638504.1:n.207-2348C>G | ||
ENST00000638568.2:c.-169+463C>G | ENSP00000491158.2:n.-169+463C>G | |
ENST00000639899.1:n.290-2348C>G | ||
ENST00000640655.2:c.-168-2348C>G | ENSP00000491596.2:n.-168-2348C>G | |
ENST00000651541.1:c.-242C>G | ENSP00000498795.1:n.-242C>G | |
ENST00000416135.5:c.-169+463C>G | ENSP00000389515.1:n.-169+463C>G | |
NM_005732.3:c.-389C>G | NP_005723.2:n.-389C>G |