HGVS | Genome Assembly |
---|---|
NC_000007.14:g.151010908G>C , CM000669.2:g.151010908G>C | GRCh38 |
NC_000007.13:g.150707996G>C , CM000669.1:g.150707996G>C | GRCh37 |
NC_000007.12:g.150338929G>C | NCBI36 |
NG_011992.1:g.24850G>C | |
NG_030317.1:g.18592C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297494.8:c.2906G>C MANE Select | ENSP00000297494.3:p.Gly969Ala | |
ENST00000297494.7:c.2906G>C | ENSP00000297494.3:p.Gly969Ala | |
ENST00000461406.5:c.2288G>C | ENSP00000417143.1:p.Gly763Ala | |
ENST00000468293.5:n.389G>C | ||
ENST00000475017.1:c.787G>C | ||
ENST00000477227.1:n.285G>C | ||
NM_000603.4:c.2906G>C | NP_000594.2:p.Gly969Ala | |
NM_000603.5:c.2906G>C MANE Select | NP_000594.2:p.Gly969Ala |