HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7533651A>G , CM000681.2:g.7533651A>G | GRCh38 |
NC_000019.9:g.7598537A>G , CM000681.1:g.7598537A>G | GRCh37 |
NC_000019.8:g.7504537A>G | NCBI36 |
NG_013374.1:g.4500A>G | |
NG_015806.1:g.16042A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264079.11:c.1704A>G MANE Select | ENSP00000264079.5:p.Gly568= | |
ENST00000264079.10:c.1704A>G | ENSP00000264079.5:p.Gly568= | |
ENST00000394321.9:n.2019A>G | ||
ENST00000599334.1:c.432A>G | ||
ENST00000601870.1:c.57A>G | ||
ENST00000602227.1:n.258A>G | ||
NM_020533.2:c.1704A>G | NP_065394.1:p.Gly568= | |
NM_020533.3:c.1704A>G MANE Select | NP_065394.1:p.Gly568= |