HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56041563A>C , CM000674.2:g.56041563A>C | GRCh38 |
NC_000012.11:g.56435347A>C , CM000674.1:g.56435347A>C | GRCh37 |
NC_000012.10:g.54721614A>C | NCBI36 |
NG_023201.1:g.4662A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356464.10:c.-357+167A>C | ENSP00000348849.5:n.-357+167A>C | |
XR_944989.1:n.150T>G | ||
XR_944990.1:n.150T>G | ||
XR_944989.3:n.441T>G | ||
XR_944990.3:n.441T>G |