Canonical Allele Identifier: CA6014984
Gene: CNTF HGNC NCBI
ZFP91-CNTF HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.58624028G>A
GRCh37 chr11:g.58391501G>A
gnomAD v2:
11:58391501 G / A
gnomAD v3:
11:58624028 G / A
gnomAD v4:
chr11-58624028-G-A
Joint Max Group AF 0.18889309 (MID)
Genomes Max Group AF 0.17108579 (AMR)
Exomes Max Group AF 0.18955889 (MID)
ClinVar RCV:
RCV000019045
ClinVar Variation:
17493
dbSNP:
1800169
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.58624028G>A , CM000673.2:g.58624028G>A GRCh38
NC_000011.9:g.58391501G>A , CM000673.1:g.58391501G>A GRCh37
NC_000011.8:g.58148077G>A NCBI36
NG_008776.1:g.6356G>A
NG_008776.2:g.6356G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361987.6:c.115-6G>A (CNTF) MANE Select ENSP00000355370.4:n.115-6G>A
ENST00000361987.5:c.115-6G>A (CNTF) ENSP00000355370.4:n.115-6G>A
ENST00000389919.8:c.*87-6G>A (ZFP91-CNTF) ENSP00000455911.1:n.*87-6G>A
ENST00000422974.2:c.1183-6G>A (ZFP91-CNTF) ENSP00000457288.1:n.1183-6G>A
NM_000614.3:c.115-6G>A (CNTF) NP_000605.1:n.115-6G>A
NR_024091.1:n.1845-6G>A (ZFP91-CNTF)
NM_000614.4:c.115-6G>A (CNTF) MANE Select NP_000605.1:n.115-6G>A
Search 100 bp 5'
Search 100 bp 3'