Canonical Allele Identifier: CA381357417

Gene: EFEMP2

Linked Data

• dbSNP Id: rs1591066116
• MyVariant Identifiers: chr11:g.65636073T>G (hg19) ; chr11:g.65868602T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868602T>G , CM000673.2:g.65868602T>G	GRCh38
NC_000011.9:g.65636073T>G , CM000673.1:g.65636073T>G	GRCh37
NC_000011.8:g.65392649T>G	NCBI36
NG_012304.2:g.9333A>C
NG_053116.1:g.13541T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.755A>C MANE Select	ENSP00000309953.6:p.Tyr252Ser
ENST00000307998.10:c.755A>C	ENSP00000309953.6:p.Tyr252Ser
ENST00000526628.5:n.1321A>C
ENST00000527969.1:n.1440A>C
ENST00000528176.5:c.755A>C	ENSP00000434151.1:p.Tyr252Ser
ENST00000531005.5:n.1749A>C
ENST00000531972.5:c.755A>C	ENSP00000435295.1:p.Tyr252Ser
ENST00000532084.5:n.181A>C
NM_016938.4:c.755A>C	NP_058634.4:p.Tyr252Ser
NR_037718.1:n.1014A>C
NM_016938.5:c.755A>C MANE Select	NP_058634.4:p.Tyr252Ser
NR_037718.2:n.880A>C