Canonical Allele Identifier: CA2574880395
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868665G>A , CM000673.2:g.65868665G>A GRCh38
NC_000011.9:g.65636136G>A , CM000673.1:g.65636136G>A GRCh37
NC_000011.8:g.65392712G>A NCBI36
NG_012304.2:g.9270C>T
NG_053116.1:g.13604G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.728-36C>T MANE Select ENSP00000309953.6:n.728-36C>T
ENST00000307998.10:c.728-36C>T ENSP00000309953.6:n.728-36C>T
ENST00000526628.5:n.1258C>T
ENST00000527969.1:n.1377C>T
ENST00000528176.5:c.728-36C>T ENSP00000434151.1:n.728-36C>T
ENST00000531005.5:n.1722-36C>T
ENST00000531972.5:c.728-36C>T ENSP00000435295.1:n.728-36C>T
ENST00000532084.5:n.154-36C>T
NM_016938.4:c.728-36C>T NP_058634.4:n.728-36C>T
NR_037718.1:n.987-36C>T
NM_016938.5:c.728-36C>T MANE Select NP_058634.4:n.728-36C>T
NR_037718.2:n.853-36C>T