Canonical Allele Identifier: CA2574880389
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868469T>C , CM000673.2:g.65868469T>C GRCh38
NC_000011.9:g.65635940T>C , CM000673.1:g.65635940T>C GRCh37
NC_000011.8:g.65392516T>C NCBI36
NG_012304.2:g.9466A>G
NG_053116.1:g.13408T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.847+41A>G MANE Select ENSP00000309953.6:n.847+41A>G
ENST00000307998.10:c.847+41A>G ENSP00000309953.6:n.847+41A>G
ENST00000526628.5:n.1413+41A>G
ENST00000528176.5:c.847+41A>G ENSP00000434151.1:n.847+41A>G
ENST00000528409.1:n.44A>G
ENST00000530806.5:c.-152+41A>G ENSP00000436526.1:n.-152+41A>G
ENST00000531005.5:n.1841+41A>G
ENST00000531972.5:c.847+41A>G ENSP00000435295.1:n.847+41A>G
ENST00000532084.5:n.273+41A>G
NM_016938.4:c.847+41A>G NP_058634.4:n.847+41A>G
NR_037718.1:n.1106+41A>G
NM_016938.5:c.847+41A>G MANE Select NP_058634.4:n.847+41A>G
NR_037718.2:n.972+41A>G