HGVS | Genome Assembly |
---|---|
NC_000006.12:g.42721826C>G , CM000668.2:g.42721826C>G | GRCh38 |
NC_000006.11:g.42689564C>G , CM000668.1:g.42689564C>G | GRCh37 |
NC_000006.10:g.42797542C>G | NCBI36 |
NG_009176.1:g.5795G>C | |
NG_009176.2:g.5795G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000230381.7:c.509G>C MANE Select | ENSP00000230381.5:p.Gly170Ala | |
ENST00000230381.6:c.509G>C | ENSP00000230381.5:p.Gly170Ala | |
NM_000322.4:c.509G>C | NP_000313.2:p.Gly170Ala | |
XR_427834.2:n.1164G>C | ||
XR_926295.1:n.1164G>C | ||
XR_427834.4:n.1214G>C | ||
XR_926295.3:n.1214G>C | ||
NM_000322.5:c.509G>C MANE Select | NP_000313.2:p.Gly170Ala |