Canonical Allele Identifier: CA2201967504
Gene: GFER HGNC NCBI

Linked Data

dbSNP Id: rs2083561820
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985693G>A , CM000678.2:g.1985693G>A GRCh38
NC_000016.9:g.2035694G>A , CM000678.1:g.2035694G>A GRCh37
NC_000016.8:g.1975695G>A NCBI36
NG_016288.1:g.6545G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.231-173G>A ENSP00000455885.1:n.231-173G>A
ENST00000248114.7:c.456-173G>A MANE Select ENSP00000248114.6:n.456-173G>A
ENST00000248114.6:c.456-173G>A ENSP00000248114.6:n.456-173G>A
ENST00000565658.1:n.613-173G>A
ENST00000567719.1:c.231-173G>A ENSP00000455885.1:n.231-173G>A
ENST00000569451.1:c.259-173G>A ENSP00000456432.1:n.259-173G>A
NM_005262.2:c.456-173G>A NP_005253.3:n.456-173G>A
NM_005262.3:c.456-173G>A MANE Select NP_005253.3:n.456-173G>A
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