HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94762632T>G , CM000672.2:g.94762632T>G | GRCh38 |
NC_000010.10:g.96522389T>G , CM000672.1:g.96522389T>G | GRCh37 |
NC_000010.9:g.96512379T>G | NCBI36 |
NG_008384.2:g.4927T>G | |
NG_008384.3:g.4952T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.7:c.-74T>G | ENSP00000360372.3:n.-74T>G | |
ENST00000464755.1:c.932-12426T>G | ENSP00000483243.1:n.932-12426T>G |