HGVS | Genome Assembly |
---|---|
NC_000006.12:g.42721894A>C , CM000668.2:g.42721894A>C | GRCh38 |
NC_000006.11:g.42689632A>C , CM000668.1:g.42689632A>C | GRCh37 |
NC_000006.10:g.42797610A>C | NCBI36 |
NG_009176.1:g.5727T>G | |
NG_009176.2:g.5727T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000230381.7:c.441T>G MANE Select | ENSP00000230381.5:p.Pro147= | |
ENST00000230381.6:c.441T>G | ENSP00000230381.5:p.Pro147= | |
NM_000322.4:c.441T>G | NP_000313.2:p.Pro147= | |
XR_427834.2:n.1096T>G | ||
XR_926295.1:n.1096T>G | ||
XR_427834.4:n.1146T>G | ||
XR_926295.3:n.1146T>G | ||
NM_000322.5:c.441T>G MANE Select | NP_000313.2:p.Pro147= |