HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226730A>C , CM000673.2:g.5226730A>C | GRCh38 |
NC_000011.9:g.5247960A>C , CM000673.1:g.5247960A>C | GRCh37 |
NC_000011.8:g.5204536A>C | NCBI36 |
NG_000007.3:g.70886T>G | |
NG_059281.1:g.5342T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.162T>G | ENSP00000494175.1:p.Ala54= | |
ENST00000335295.4:c.162T>G MANE Select | ENSP00000333994.3:p.Ala54= | |
ENST00000380315.2:c.162T>G | ENSP00000369671.2:p.Ala54= | |
ENST00000475226.1:n.94T>G | ||
ENST00000485743.1:n.213T>G | ||
ENST00000633227.1:c.146T>G | ENSP00000488004.1:p.Leu49Arg | |
NM_000518.4:c.162T>G | NP_000509.1:p.Ala54= | |
NM_000518.5:c.162T>G MANE Select | NP_000509.1:p.Ala54= |