HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94762645A>T , CM000672.2:g.94762645A>T | GRCh38 |
NC_000010.10:g.96522402A>T , CM000672.1:g.96522402A>T | GRCh37 |
NC_000010.9:g.96512392A>T | NCBI36 |
NG_008384.2:g.4940A>T | |
NG_008384.3:g.4965A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.7:c.-61A>T | ENSP00000360372.3:n.-61A>T | |
ENST00000464755.1:c.932-12413A>T | ENSP00000483243.1:n.932-12413A>T |