Canonical Allele Identifier: CA381357275
Gene: EFEMP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868596C>G , CM000673.2:g.65868596C>G GRCh38
NC_000011.9:g.65636067C>G , CM000673.1:g.65636067C>G GRCh37
NC_000011.8:g.65392643C>G NCBI36
NG_012304.2:g.9339G>C
NG_053116.1:g.13535C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.761G>C MANE Select ENSP00000309953.6:p.Cys254Ser
ENST00000307998.10:c.761G>C ENSP00000309953.6:p.Cys254Ser
ENST00000526628.5:n.1327G>C
ENST00000527969.1:n.1446G>C
ENST00000528176.5:c.761G>C ENSP00000434151.1:p.Cys254Ser
ENST00000531005.5:n.1755G>C
ENST00000531972.5:c.761G>C ENSP00000435295.1:p.Cys254Ser
ENST00000532084.5:n.187G>C
NM_016938.4:c.761G>C NP_058634.4:p.Cys254Ser
NR_037718.1:n.1020G>C
NM_016938.5:c.761G>C MANE Select NP_058634.4:p.Cys254Ser
NR_037718.2:n.886G>C