Canonical Allele Identifier: CA1043460915
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs1692052906
gnomAD v3: 2-232543168-G-C
gnomAD v4: 2-232543168-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543168G>C , CM000664.2:g.232543168G>C GRCh38
NC_000002.11:g.233407878G>C , CM000664.1:g.233407878G>C GRCh37
NC_000002.10:g.233116122G>C NCBI36
NG_012954.1:g.8442G>C
NG_012954.2:g.8477G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.805+86G>C MANE Select ENSP00000498757.1:n.805+86G>C
ENST00000389492.3:c.649+86G>C ENSP00000374143.3:n.649+86G>C
ENST00000389494.7:c.805+86G>C ENSP00000374145.3:n.805+86G>C
NM_005199.4:c.805+86G>C NP_005190.4:n.805+86G>C
NM_005199.5:c.805+86G>C MANE Select NP_005190.4:n.805+86G>C
Search 100 bp 5'
Search 100 bp 3'