HGVS | Genome Assembly |
---|---|
NC_000020.11:g.44115623T>C , CM000682.2:g.44115623T>C | GRCh38 |
NC_000020.10:g.42744263T>C , CM000682.1:g.42744263T>C | GRCh37 |
NC_000020.9:g.42177677T>C | NCBI36 |
NG_031867.1:g.76956A>G , LRG_394:g.76956A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372980.4:c.2010+42A>G MANE Select | ENSP00000362071.3:n.2010+42A>G | |
ENST00000372980.3:c.2010+42A>G | ENSP00000362071.3:n.2010+42A>G | |
NM_020433.4:c.2010+42A>G , LRG_394t1:c.2010+42A>G | NP_065166.2:n.2010+42A>G | |
XM_006723832.2:c.2010+42A>G | XP_006723895.1:n.2010+42A>G | |
NM_020433.5:c.2010+42A>G MANE Select | NP_065166.2:n.2010+42A>G |