Canonical Allele Identifier: CA2663621589
Gene: CHRNG HGNC NCBI

Linked Data

gnomAD v4: 2-232539978-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539978C>T , CM000664.2:g.232539978C>T GRCh38
NC_000002.11:g.233404688C>T , CM000664.1:g.233404688C>T GRCh37
NC_000002.10:g.233112932C>T NCBI36
NG_012954.1:g.5252C>T
NG_012954.2:g.5287C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.56-14C>T MANE Select ENSP00000498757.1:n.56-14C>T
ENST00000389492.3:c.56-14C>T ENSP00000374143.3:n.56-14C>T
ENST00000389494.7:c.56-14C>T ENSP00000374145.3:n.56-14C>T
ENST00000485094.1:n.77-14C>T
NM_005199.4:c.56-14C>T NP_005190.4:n.56-14C>T
NM_005199.5:c.56-14C>T MANE Select NP_005190.4:n.56-14C>T
Search 100 bp 5'
Search 100 bp 3'