HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551489C>T , CM000681.2:g.43551489C>T | GRCh38 |
NC_000019.9:g.44055641C>T , CM000681.1:g.44055641C>T | GRCh37 |
NC_000019.8:g.48747481C>T | NCBI36 |
NG_033799.1:g.29090G>A , LRG_784:g.29090G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262887.10:c.1199+82G>A MANE Select | ENSP00000262887.5:n.1199+82G>A | |
ENST00000262887.9:c.1199+82G>A | ENSP00000262887.4:n.1199+82G>A | |
ENST00000543982.5:c.1106+82G>A | ENSP00000443671.1:n.1106+82G>A | |
NM_006297.2:c.1199+82G>A , LRG_784t1:c.1199+82G>A | NP_006288.2:n.1199+82G>A | |
NM_006297.3:c.1199+82G>A MANE Select | NP_006288.2:n.1199+82G>A |