HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19960857A>G , CM000670.2:g.19960857A>G | GRCh38 |
NC_000008.10:g.19818368A>G , CM000670.1:g.19818368A>G | GRCh37 |
NC_000008.9:g.19862648A>G | NCBI36 |
NG_008855.1:g.26787A>G | |
NG_008855.2:g.64141A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.1140-44A>G MANE Select | ENSP00000497642.1:n.1140-44A>G | |
ENST00000650478.1:c.80-44A>G | ENSP00000497560.1:n.80-44A>G | |
ENST00000311322.8:c.1140-44A>G | ENSP00000309757.6:n.1140-44A>G | |
NM_000237.2:c.1140-44A>G | NP_000228.1:n.1140-44A>G | |
NM_000237.3:c.1140-44A>G MANE Select | NP_000228.1:n.1140-44A>G |