Canonical Allele Identifier: CA2792462173
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868692A>G , CM000673.2:g.65868692A>G GRCh38
NC_000011.9:g.65636163A>G , CM000673.1:g.65636163A>G GRCh37
NC_000011.8:g.65392739A>G NCBI36
NG_012304.2:g.9243T>C
NG_053116.1:g.13631A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.728-63T>C MANE Select ENSP00000309953.6:n.728-63T>C
ENST00000307998.10:c.728-63T>C ENSP00000309953.6:n.728-63T>C
ENST00000526628.5:n.1231T>C
ENST00000527969.1:n.1350T>C
ENST00000528176.5:c.728-63T>C ENSP00000434151.1:n.728-63T>C
ENST00000531005.5:n.1722-63T>C
ENST00000531972.5:c.728-63T>C ENSP00000435295.1:n.728-63T>C
ENST00000532084.5:n.154-63T>C
NM_016938.4:c.728-63T>C NP_058634.4:n.728-63T>C
NR_037718.1:n.987-63T>C
NM_016938.5:c.728-63T>C MANE Select NP_058634.4:n.728-63T>C
NR_037718.2:n.853-63T>C