HGVS | Genome Assembly |
---|---|
NC_000023.11:g.30308332T>C , CM000685.2:g.30308332T>C | GRCh38 |
NC_000023.10:g.30326449T>C , CM000685.1:g.30326449T>C | GRCh37 |
NC_000023.9:g.30236370T>C | NCBI36 |
NG_009814.1:g.6047A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378970.5:c.1032A>G MANE Select | ENSP00000368253.4:p.Ala344= | |
ENST00000378963.1:c.147A>G | ENSP00000368246.1:p.Ala49= | |
ENST00000378970.4:c.1032A>G | ENSP00000368253.4:p.Ala344= | |
NM_000475.4:c.1032A>G | NP_000466.2:p.Ala344= | |
NM_000475.5:c.1032A>G MANE Select | NP_000466.2:p.Ala344= |