Canonical Allele Identifier: CA394303894
Gene: GFER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985899G>T , CM000678.2:g.1985899G>T GRCh38
NC_000016.9:g.2035900G>T , CM000678.1:g.2035900G>T GRCh37
NC_000016.8:g.1975901G>T NCBI36
NG_016288.1:g.6751G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.264G>T ENSP00000455885.1:p.Arg88=
ENST00000248114.7:c.489G>T MANE Select ENSP00000248114.6:p.Arg163=
ENST00000248114.6:c.489G>T ENSP00000248114.6:p.Arg163=
ENST00000565658.1:n.646G>T
ENST00000567719.1:c.264G>T ENSP00000455885.1:p.Arg88=
ENST00000569451.1:c.292G>T ENSP00000456432.1:p.Gly98Cys
NM_005262.2:c.489G>T NP_005253.3:p.Arg163=
NM_005262.3:c.489G>T MANE Select NP_005253.3:p.Arg163=