HGVS | Genome Assembly |
---|---|
NC_000009.12:g.82521969A>G , CM000671.2:g.82521969A>G | GRCh38 |
NC_000009.11:g.85136884A>G , CM000671.1:g.85136884A>G | GRCh37 |
NC_000009.10:g.84326704A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000589973.2:n.247+25111A>G | ||
ENST00000590298.5:n.440-42060A>G | ||
ENST00000590791.5:n.526-2550A>G | ||
ENST00000591257.5:n.347-2550A>G | ||
ENST00000637606.1:n.985+25111A>G | ||
XR_001746782.1:n.241+25111A>G |