Canonical Allele Identifier: CA475316885

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65636081G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868610G>A , CM000673.2:g.65868610G>A	GRCh38
NC_000011.9:g.65636081G>A , CM000673.1:g.65636081G>A	GRCh37
NC_000011.8:g.65392657G>A	NCBI36
NG_012304.2:g.9325C>T
NG_053116.1:g.13549G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.747C>T MANE Select	ENSP00000309953.6:p.Tyr249=
ENST00000307998.10:c.747C>T	ENSP00000309953.6:p.Tyr249=
ENST00000526628.5:n.1313C>T
ENST00000527969.1:n.1432C>T
ENST00000528176.5:c.747C>T	ENSP00000434151.1:p.Tyr249=
ENST00000531005.5:n.1741C>T
ENST00000531972.5:c.747C>T	ENSP00000435295.1:p.Tyr249=
ENST00000532084.5:n.173C>T
NM_016938.4:c.747C>T	NP_058634.4:p.Tyr249=
NR_037718.1:n.1006C>T
NM_016938.5:c.747C>T MANE Select	NP_058634.4:p.Tyr249=
NR_037718.2:n.872C>T