Canonical Allele Identifier: CA2976483621
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65871396C>G , CM000673.2:g.65871396C>G GRCh38
NC_000011.9:g.65638867C>G , CM000673.1:g.65638867C>G GRCh37
NC_000011.8:g.65395443C>G NCBI36
NG_012304.2:g.6539G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.161-33G>C MANE Select ENSP00000309953.6:n.161-33G>C
ENST00000307998.10:c.161-33G>C ENSP00000309953.6:n.161-33G>C
ENST00000526624.5:c.161-33G>C ENSP00000435419.1:n.161-33G>C
ENST00000527378.1:c.161-33G>C ENSP00000435963.1:n.161-33G>C
ENST00000528176.5:c.161-33G>C ENSP00000434151.1:n.161-33G>C
ENST00000530850.1:c.150-33G>C ENSP00000437238.1:n.150-33G>C
ENST00000531005.5:n.624G>C
ENST00000531972.5:c.161-33G>C ENSP00000435295.1:n.161-33G>C
ENST00000533347.5:c.174G>C ENSP00000435823.1:p.Glu58Asp
NM_016938.4:c.161-33G>C NP_058634.4:n.161-33G>C
NR_037718.1:n.420-33G>C
NM_016938.5:c.161-33G>C MANE Select NP_058634.4:n.161-33G>C
NR_037718.2:n.286-33G>C