HGVS | Genome Assembly |
---|---|
NC_000009.12:g.127800442T>C , CM000671.2:g.127800442T>C | GRCh38 |
NC_000009.11:g.130562721T>C , CM000671.1:g.130562721T>C | GRCh37 |
NC_000009.10:g.129602542T>C | NCBI36 |
NG_023245.1:g.2568T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000479147.6:n.217-3843T>C | ||
ENST00000479375.6:n.132-3843T>C |