Canonical Allele Identifier: CA431809475
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233404715G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232540005G>T , CM000664.2:g.232540005G>T GRCh38
NC_000002.11:g.233404715G>T , CM000664.1:g.233404715G>T GRCh37
NC_000002.10:g.233112959G>T NCBI36
NG_012954.1:g.5279G>T
NG_012954.2:g.5314G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.69G>T MANE Select ENSP00000498757.1:p.Arg23=
ENST00000389492.3:c.69G>T ENSP00000374143.3:p.Arg23=
ENST00000389494.7:c.69G>T ENSP00000374145.3:p.Arg23=
ENST00000485094.1:n.90G>T
NM_005199.4:c.69G>T NP_005190.4:p.Arg23=
NM_005199.5:c.69G>T MANE Select NP_005190.4:p.Arg23=