Canonical Allele Identifier: CA2614412923

Gene: EFEMP2

Linked Data

• gnomAD v4: 11-65871413-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65871413G>C , CM000673.2:g.65871413G>C	GRCh38
NC_000011.9:g.65638884G>C , CM000673.1:g.65638884G>C	GRCh37
NC_000011.8:g.65395460G>C	NCBI36
NG_012304.2:g.6522C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.161-50C>G MANE Select	ENSP00000309953.6:n.161-50C>G
ENST00000307998.10:c.161-50C>G	ENSP00000309953.6:n.161-50C>G
ENST00000526624.5:c.161-50C>G	ENSP00000435419.1:n.161-50C>G
ENST00000527378.1:c.161-50C>G	ENSP00000435963.1:n.161-50C>G
ENST00000528176.5:c.161-50C>G	ENSP00000434151.1:n.161-50C>G
ENST00000530850.1:c.150-50C>G	ENSP00000437238.1:n.150-50C>G
ENST00000531005.5:n.607C>G
ENST00000531972.5:c.161-50C>G	ENSP00000435295.1:n.161-50C>G
ENST00000533347.5:c.161-4C>G	ENSP00000435823.1:n.161-4C>G
NM_016938.4:c.161-50C>G	NP_058634.4:n.161-50C>G
NR_037718.1:n.420-50C>G
NM_016938.5:c.161-50C>G MANE Select	NP_058634.4:n.161-50C>G
NR_037718.2:n.286-50C>G