Canonical Allele Identifier: CA2614405473
Gene: EFEMP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868443G>A , CM000673.2:g.65868443G>A GRCh38
NC_000011.9:g.65635914G>A , CM000673.1:g.65635914G>A GRCh37
NC_000011.8:g.65392490G>A NCBI36
NG_012304.2:g.9492C>T
NG_053116.1:g.13382G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.848-22C>T MANE Select ENSP00000309953.6:n.848-22C>T
ENST00000307998.10:c.848-22C>T ENSP00000309953.6:n.848-22C>T
ENST00000526628.5:n.1414-22C>T
ENST00000528176.5:c.848-22C>T ENSP00000434151.1:n.848-22C>T
ENST00000528409.1:n.70C>T
ENST00000530806.5:c.-151-22C>T ENSP00000436526.1:n.-151-22C>T
ENST00000531005.5:n.1842-22C>T
ENST00000531972.5:c.848-22C>T ENSP00000435295.1:n.848-22C>T
ENST00000532084.5:n.274-22C>T
NM_016938.4:c.848-22C>T NP_058634.4:n.848-22C>T
NR_037718.1:n.1107-22C>T
NM_016938.5:c.848-22C>T MANE Select NP_058634.4:n.848-22C>T
NR_037718.2:n.973-22C>T