HGVS | Genome Assembly |
---|---|
NC_000007.14:g.100647080G>C , CM000669.2:g.100647080G>C | GRCh38 |
NC_000007.13:g.100244703G>C , CM000669.1:g.100244703G>C | GRCh37 |
NC_000007.12:g.100082639G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000160382.10:c.827C>G MANE Select | ENSP00000160382.5:p.Ala276Gly | |
ENST00000160382.9:c.827C>G | ENSP00000160382.5:p.Ala276Gly | |
ENST00000487125.1:n.389C>G | ||
NM_016188.4:c.827C>G | NP_057272.1:p.Ala276Gly | |
XR_927476.1:n.934C>G | ||
NR_134539.1:n.934C>G | ||
NM_016188.5:c.827C>G MANE Select | NP_057272.1:p.Ala276Gly | |
NR_134539.2:n.921C>G |