Canonical Allele Identifier: CA492950316
Gene: GFER HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2036017C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1986016C>A , CM000678.2:g.1986016C>A GRCh38
NC_000016.9:g.2036017C>A , CM000678.1:g.2036017C>A GRCh37
NC_000016.8:g.1976018C>A NCBI36
NG_016288.1:g.6868C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.381C>A ENSP00000455885.1:p.Gly127=
ENST00000248114.7:c.606C>A MANE Select ENSP00000248114.6:p.Gly202=
ENST00000248114.6:c.606C>A ENSP00000248114.6:p.Gly202=
ENST00000565658.1:n.763C>A
ENST00000567719.1:c.381C>A ENSP00000455885.1:p.Gly127=
ENST00000569451.1:c.*79C>A ENSP00000456432.1:n.*79C>A
NM_005262.2:c.606C>A NP_005253.3:p.Gly202=
NM_005262.3:c.606C>A MANE Select NP_005253.3:p.Gly202=
Search 100 bp 5'
Search 100 bp 3'