Canonical Allele Identifier: CA381357478

Gene: EFEMP2

Linked Data

• gnomAD v4: 11-65868606-T-C
• MyVariant Identifiers: chr11:g.65636077T>C (hg19) ; chr11:g.65868606T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868606T>C , CM000673.2:g.65868606T>C	GRCh38
NC_000011.9:g.65636077T>C , CM000673.1:g.65636077T>C	GRCh37
NC_000011.8:g.65392653T>C	NCBI36
NG_012304.2:g.9329A>G
NG_053116.1:g.13545T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.751A>G MANE Select	ENSP00000309953.6:p.Ser251Gly
ENST00000307998.10:c.751A>G	ENSP00000309953.6:p.Ser251Gly
ENST00000526628.5:n.1317A>G
ENST00000527969.1:n.1436A>G
ENST00000528176.5:c.751A>G	ENSP00000434151.1:p.Ser251Gly
ENST00000531005.5:n.1745A>G
ENST00000531972.5:c.751A>G	ENSP00000435295.1:p.Ser251Gly
ENST00000532084.5:n.177A>G
NM_016938.4:c.751A>G	NP_058634.4:p.Ser251Gly
NR_037718.1:n.1010A>G
NM_016938.5:c.751A>G MANE Select	NP_058634.4:p.Ser251Gly
NR_037718.2:n.876A>G