HGVS | Genome Assembly |
---|---|
NC_000005.10:g.132527285T>A , CM000667.2:g.132527285T>A | GRCh38 |
NC_000005.9:g.131862977T>A , CM000667.1:g.131862977T>A | GRCh37 |
NC_000005.8:g.131890876T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000638452.2:c.-168-31999T>A | ENSP00000492349.2:n.-168-31999T>A | |
ENST00000638504.1:n.207-31999T>A | ||
ENST00000638568.2:c.-310-29047T>A | ENSP00000491158.2:n.-310-29047T>A | |
ENST00000639899.1:n.290-31999T>A | ||
ENST00000640655.2:c.-168-31999T>A | ENSP00000491596.2:n.-168-31999T>A |