HGVS | Genome Assembly |
---|---|
NC_000001.11:g.87147675T>G , CM000663.2:g.87147675T>G | GRCh38 |
NC_000001.10:g.87613358T>G , CM000663.1:g.87613358T>G | GRCh37 |
NC_000001.9:g.87385946T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370548.3:c.871+13957T>G | ENSP00000359579.1:n.871+13957T>G | |
NR_026989.1:n.335+13957T>G |