HGVS | Genome Assembly |
---|---|
NC_000009.12:g.82521000A>T , CM000671.2:g.82521000A>T | GRCh38 |
NC_000009.11:g.85135915A>T , CM000671.1:g.85135915A>T | GRCh37 |
NC_000009.10:g.84325735A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000589973.2:n.247+24142A>T | ||
ENST00000590298.5:n.440-43029A>T | ||
ENST00000590791.5:n.526-3519A>T | ||
ENST00000591257.5:n.347-3519A>T | ||
ENST00000637606.1:n.985+24142A>T | ||
XR_001746782.1:n.241+24142A>T |