Canonical Allele Identifier: CA394303789
Gene: GFER HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2035887A>G (hg19) chr16:g.1985886A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985886A>G , CM000678.2:g.1985886A>G GRCh38
NC_000016.9:g.2035887A>G , CM000678.1:g.2035887A>G GRCh37
NC_000016.8:g.1975888A>G NCBI36
NG_016288.1:g.6738A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.251A>G ENSP00000455885.1:p.Asp84Gly
ENST00000248114.7:c.476A>G MANE Select ENSP00000248114.6:p.Asp159Gly
ENST00000248114.6:c.476A>G ENSP00000248114.6:p.Asp159Gly
ENST00000565658.1:n.633A>G
ENST00000567719.1:c.251A>G ENSP00000455885.1:p.Asp84Gly
ENST00000569451.1:c.279A>G ENSP00000456432.1:p.Arg93=
NM_005262.2:c.476A>G NP_005253.3:p.Asp159Gly
NM_005262.3:c.476A>G MANE Select NP_005253.3:p.Asp159Gly
Search 100 bp 5'
Search 100 bp 3'