Canonical Allele Identifier: CA183009
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65870669C>T , CM000673.2:g.65870669C>T GRCh38
NC_000011.9:g.65638140C>T , CM000673.1:g.65638140C>T GRCh37
NC_000011.8:g.65394716C>T NCBI36
NG_012304.2:g.7266G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.368-11G>A MANE Select ENSP00000309953.6:n.368-11G>A
ENST00000307998.10:c.368-11G>A ENSP00000309953.6:n.368-11G>A
ENST00000526624.5:c.368-11G>A ENSP00000435419.1:n.368-11G>A
ENST00000527378.1:c.368-11G>A ENSP00000435963.1:n.368-11G>A
ENST00000527969.1:n.47-11G>A
ENST00000528176.5:c.368-11G>A ENSP00000434151.1:n.368-11G>A
ENST00000530850.1:c.*180-11G>A ENSP00000437238.1:n.*180-11G>A
ENST00000531005.5:n.1351G>A
ENST00000531972.5:c.368-11G>A ENSP00000435295.1:n.368-11G>A
ENST00000533347.5:c.*180-11G>A ENSP00000435823.1:n.*180-11G>A
NM_016938.4:c.368-11G>A NP_058634.4:n.368-11G>A
NR_037718.1:n.627-11G>A
NM_016938.5:c.368-11G>A MANE Select NP_058634.4:n.368-11G>A
NR_037718.2:n.493-11G>A