Canonical Allele Identifier: CA381356728
Gene: EFEMP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.65636032A>C (hg19) chr11:g.65868561A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868561A>C , CM000673.2:g.65868561A>C GRCh38
NC_000011.9:g.65636032A>C , CM000673.1:g.65636032A>C GRCh37
NC_000011.8:g.65392608A>C NCBI36
NG_012304.2:g.9374T>G
NG_053116.1:g.13500A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.796T>G MANE Select ENSP00000309953.6:p.Ser266Ala
ENST00000307998.10:c.796T>G ENSP00000309953.6:p.Ser266Ala
ENST00000526628.5:n.1362T>G
ENST00000527969.1:n.1481T>G
ENST00000528176.5:c.796T>G ENSP00000434151.1:p.Ser266Ala
ENST00000531005.5:n.1790T>G
ENST00000531972.5:c.796T>G ENSP00000435295.1:p.Ser266Ala
ENST00000532084.5:n.222T>G
NM_016938.4:c.796T>G NP_058634.4:p.Ser266Ala
NR_037718.1:n.1055T>G
NM_016938.5:c.796T>G MANE Select NP_058634.4:p.Ser266Ala
NR_037718.2:n.921T>G
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