Canonical Allele Identifier: CA766142688
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs2853460
gnomAD v3: 2-232541344-C-T
gnomAD v4: 2-232541344-C-T
MyVariant Identifiers: chr2:g.233406054C>T (hg19) chr2:g.232541344C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541344C>T , CM000664.2:g.232541344C>T GRCh38
NC_000002.11:g.233406054C>T , CM000664.1:g.233406054C>T GRCh37
NC_000002.10:g.233114298C>T NCBI36
NG_012954.1:g.6618C>T
NG_012954.2:g.6653C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.351-30C>T MANE Select ENSP00000498757.1:n.351-30C>T
ENST00000389492.3:c.350+633C>T ENSP00000374143.3:n.350+633C>T
ENST00000389494.7:c.351-30C>T ENSP00000374145.3:n.351-30C>T
ENST00000485094.1:n.372-30C>T
NM_005199.4:c.351-30C>T NP_005190.4:n.351-30C>T
NM_005199.5:c.351-30C>T MANE Select NP_005190.4:n.351-30C>T
Search 100 bp 5'
Search 100 bp 3'