Canonical Allele Identifier: CA1979444940
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65871298C= , CM000673.2:g.65871298C= GRCh38
NC_000011.9:g.65638769C= , CM000673.1:g.65638769C= GRCh37
NC_000011.8:g.65395345C= NCBI36
NG_012304.2:g.6637G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.226G= MANE Select ENSP00000309953.6:p.Gly76=
ENST00000307998.10:c.226G= ENSP00000309953.6:p.Gly76=
ENST00000526624.5:c.226G= ENSP00000435419.1:p.Gly76=
ENST00000527378.1:c.226G= ENSP00000435963.1:p.Gly76=
ENST00000528176.5:c.226G= ENSP00000434151.1:p.Gly76=
ENST00000530850.1:c.*38G= ENSP00000437238.1:n.*38G=
ENST00000531005.5:n.722G=
ENST00000531972.5:c.226G= ENSP00000435295.1:p.Gly76=
ENST00000533347.5:c.*38G= ENSP00000435823.1:n.*38G=
NM_016938.4:c.226G= NP_058634.4:p.Gly76=
NR_037718.1:n.485G=
NM_016938.5:c.226G= MANE Select NP_058634.4:p.Gly76=
NR_037718.2:n.351G=