Canonical Allele Identifier: CA276773501
Gene: GFER HGNC NCBI

Linked Data

dbSNP Id: rs371922095
MyVariant Identifiers: chr16:g.2035928C>G (hg19) chr16:g.1985927C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985927C>G , CM000678.2:g.1985927C>G GRCh38
NC_000016.9:g.2035928C>G , CM000678.1:g.2035928C>G GRCh37
NC_000016.8:g.1975929C>G NCBI36
NG_016288.1:g.6779C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.292C>G ENSP00000455885.1:p.Leu98Val
ENST00000248114.7:c.517C>G MANE Select ENSP00000248114.6:p.Leu173Val
ENST00000248114.6:c.517C>G ENSP00000248114.6:p.Leu173Val
ENST00000565658.1:n.674C>G
ENST00000567719.1:c.292C>G ENSP00000455885.1:p.Leu98Val
ENST00000569451.1:c.320C>G ENSP00000456432.1:p.Pro107Arg
NM_005262.2:c.517C>G NP_005253.3:p.Leu173Val
NM_005262.3:c.517C>G MANE Select NP_005253.3:p.Leu173Val
Search 100 bp 5'
Search 100 bp 3'