Canonical Allele Identifier: CA2614413003

Gene: EFEMP2

Linked Data

• gnomAD v4: 11-65871461-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65871461C>G , CM000673.2:g.65871461C>G	GRCh38
NC_000011.9:g.65638932C>G , CM000673.1:g.65638932C>G	GRCh37
NC_000011.8:g.65395508C>G	NCBI36
NG_012304.2:g.6474G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.161-98G>C MANE Select	ENSP00000309953.6:n.161-98G>C
ENST00000307998.10:c.161-98G>C	ENSP00000309953.6:n.161-98G>C
ENST00000526624.5:c.161-98G>C	ENSP00000435419.1:n.161-98G>C
ENST00000527378.1:c.161-98G>C	ENSP00000435963.1:n.161-98G>C
ENST00000528176.5:c.161-98G>C	ENSP00000434151.1:n.161-98G>C
ENST00000529870.1:n.766G>C
ENST00000530850.1:c.150-98G>C	ENSP00000437238.1:n.150-98G>C
ENST00000531005.5:n.559G>C
ENST00000531972.5:c.161-98G>C	ENSP00000435295.1:n.161-98G>C
ENST00000533347.5:c.161-52G>C	ENSP00000435823.1:n.161-52G>C
NM_016938.4:c.161-98G>C	NP_058634.4:n.161-98G>C
NR_037718.1:n.420-98G>C
NM_016938.5:c.161-98G>C MANE Select	NP_058634.4:n.161-98G>C
NR_037718.2:n.286-98G>C