Canonical Allele Identifier: CA66968807
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs566102476
gnomAD v3: 2-232543194-C-T
gnomAD v4: 2-232543194-C-T
MyVariant Identifiers: chr2:g.233407904C>T (hg19) chr2:g.232543194C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543194C>T , CM000664.2:g.232543194C>T GRCh38
NC_000002.11:g.233407904C>T , CM000664.1:g.233407904C>T GRCh37
NC_000002.10:g.233116148C>T NCBI36
NG_012954.1:g.8468C>T
NG_012954.2:g.8503C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.806-81C>T MANE Select ENSP00000498757.1:n.806-81C>T
ENST00000389492.3:c.650-81C>T ENSP00000374143.3:n.650-81C>T
ENST00000389494.7:c.806-81C>T ENSP00000374145.3:n.806-81C>T
NM_005199.4:c.806-81C>T NP_005190.4:n.806-81C>T
NM_005199.5:c.806-81C>T MANE Select NP_005190.4:n.806-81C>T
Search 100 bp 5'
Search 100 bp 3'