Canonical Allele Identifier: CA381354318

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65635980C>T (hg19) ; chr11:g.65868509C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868509C>T , CM000673.2:g.65868509C>T	GRCh38
NC_000011.9:g.65635980C>T , CM000673.1:g.65635980C>T	GRCh37
NC_000011.8:g.65392556C>T	NCBI36
NG_012304.2:g.9426G>A
NG_053116.1:g.13448C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.847+1G>A MANE Select	ENSP00000309953.6:n.847+1G>A
ENST00000307998.10:c.847+1G>A	ENSP00000309953.6:n.847+1G>A
ENST00000526628.5:n.1413+1G>A
ENST00000527969.1:n.1533G>A
ENST00000528176.5:c.847+1G>A	ENSP00000434151.1:n.847+1G>A
ENST00000528409.1:n.4G>A
ENST00000530806.5:c.-152+1G>A	ENSP00000436526.1:n.-152+1G>A
ENST00000531005.5:n.1841+1G>A
ENST00000531972.5:c.847+1G>A	ENSP00000435295.1:n.847+1G>A
ENST00000532084.5:n.273+1G>A
NM_016938.4:c.847+1G>A	NP_058634.4:n.847+1G>A
NR_037718.1:n.1106+1G>A
NM_016938.5:c.847+1G>A MANE Select	NP_058634.4:n.847+1G>A
NR_037718.2:n.972+1G>A