HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551542A>G , CM000681.2:g.43551542A>G | GRCh38 |
NC_000019.9:g.44055694A>G , CM000681.1:g.44055694A>G | GRCh37 |
NC_000019.8:g.48747534A>G | NCBI36 |
NG_033799.1:g.29037T>C , LRG_784:g.29037T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.1199+29T>C MANE Select | ENSP00000262887.5:n.1199+29T>C | |
ENST00000262887.9:c.1199+29T>C | ENSP00000262887.4:n.1199+29T>C | |
ENST00000543982.5:c.1106+29T>C | ENSP00000443671.1:n.1106+29T>C | |
NM_006297.2:c.1199+29T>C , LRG_784t1:c.1199+29T>C | NP_006288.2:n.1199+29T>C | |
NM_006297.3:c.1199+29T>C MANE Select | NP_006288.2:n.1199+29T>C |