Canonical Allele Identifier: CA276773462
Gene: GFER HGNC NCBI

Linked Data

dbSNP Id: rs571386314
MyVariant Identifiers: chr16:g.2035856T>A (hg19) chr16:g.1985855T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985855T>A , CM000678.2:g.1985855T>A GRCh38
NC_000016.9:g.2035856T>A , CM000678.1:g.2035856T>A GRCh37
NC_000016.8:g.1975857T>A NCBI36
NG_016288.1:g.6707T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.231-11T>A ENSP00000455885.1:n.231-11T>A
ENST00000248114.7:c.456-11T>A MANE Select ENSP00000248114.6:n.456-11T>A
ENST00000248114.6:c.456-11T>A ENSP00000248114.6:n.456-11T>A
ENST00000565658.1:n.613-11T>A
ENST00000567719.1:c.231-11T>A ENSP00000455885.1:n.231-11T>A
ENST00000569451.1:c.259-11T>A ENSP00000456432.1:n.259-11T>A
NM_005262.2:c.456-11T>A NP_005253.3:n.456-11T>A
NM_005262.3:c.456-11T>A MANE Select NP_005253.3:n.456-11T>A
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