Canonical Allele Identifier: CA381356823

Gene: EFEMP2

Linked Data

• dbSNP Id: rs1212797548
• MyVariant Identifiers: chr11:g.65636038G>C (hg19) ; chr11:g.65868567G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868567G>C , CM000673.2:g.65868567G>C	GRCh38
NC_000011.9:g.65636038G>C , CM000673.1:g.65636038G>C	GRCh37
NC_000011.8:g.65392614G>C	NCBI36
NG_012304.2:g.9368C>G
NG_053116.1:g.13506G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.790C>G MANE Select	ENSP00000309953.6:p.Arg264Gly
ENST00000307998.10:c.790C>G	ENSP00000309953.6:p.Arg264Gly
ENST00000526628.5:n.1356C>G
ENST00000527969.1:n.1475C>G
ENST00000528176.5:c.790C>G	ENSP00000434151.1:p.Arg264Gly
ENST00000531005.5:n.1784C>G
ENST00000531972.5:c.790C>G	ENSP00000435295.1:p.Arg264Gly
ENST00000532084.5:n.216C>G
NM_016938.4:c.790C>G	NP_058634.4:p.Arg264Gly
NR_037718.1:n.1049C>G
NM_016938.5:c.790C>G MANE Select	NP_058634.4:p.Arg264Gly
NR_037718.2:n.915C>G