Canonical Allele Identifier: CA223152725
Gene: CNTF HGNC NCBI
ZFP91-CNTF HGNC NCBI

Linked Data

ClinVar Variation Id: 2225361
ClinVar RCV Id: RCV004090938
dbSNP Id: rs1024349725
gnomAD v3: 11-58624487-G-A
gnomAD v4: 11-58624487-G-A
MyVariant Identifiers: chr11:g.58391960G>A (hg19) chr11:g.58624487G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.58624487G>A , CM000673.2:g.58624487G>A GRCh38
NC_000011.9:g.58391960G>A , CM000673.1:g.58391960G>A GRCh37
NC_000011.8:g.58148536G>A NCBI36
NG_008776.1:g.6815G>A
NG_008776.2:g.6815G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361987.6:c.568G>A (CNTF) MANE Select ENSP00000355370.4:p.Gly190Arg
ENST00000361987.5:c.568G>A (CNTF) ENSP00000355370.4:p.Gly190Arg
ENST00000389919.8:c.*540G>A (ZFP91-CNTF) ENSP00000455911.1:n.*540G>A
ENST00000422974.2:c.1636G>A (ZFP91-CNTF) ENSP00000457288.1:n.1636G>A
NM_000614.3:c.568G>A (CNTF) NP_000605.1:p.Gly190Arg
NR_024091.1:n.2298G>A (ZFP91-CNTF)
NM_000614.4:c.568G>A (CNTF) MANE Select NP_000605.1:p.Gly190Arg
Search 100 bp 5'
Search 100 bp 3'