Canonical Allele Identifier: CA1335312203
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs1211853989
gnomAD v4: 2-232539830-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539830G>T , CM000664.2:g.232539830G>T GRCh38
NC_000002.11:g.233404540G>T , CM000664.1:g.233404540G>T GRCh37
NC_000002.10:g.233112784G>T NCBI36
NG_012954.1:g.5104G>T
NG_012954.2:g.5139G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.55+28G>T MANE Select ENSP00000498757.1:n.55+28G>T
ENST00000389492.3:c.55+28G>T ENSP00000374143.3:n.55+28G>T
ENST00000389494.7:c.55+28G>T ENSP00000374145.3:n.55+28G>T
ENST00000485094.1:n.76+28G>T
NM_005199.4:c.55+28G>T NP_005190.4:n.55+28G>T
NM_005199.5:c.55+28G>T MANE Select NP_005190.4:n.55+28G>T
Search 100 bp 5'
Search 100 bp 3'