Canonical Allele Identifier: CA351008439
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233406106G>C (hg19) chr2:g.232541396G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541396G>C , CM000664.2:g.232541396G>C GRCh38
NC_000002.11:g.233406106G>C , CM000664.1:g.233406106G>C GRCh37
NC_000002.10:g.233114350G>C NCBI36
NG_012954.1:g.6670G>C
NG_012954.2:g.6705G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.373G>C MANE Select ENSP00000498757.1:p.Ala125Pro
ENST00000389492.3:c.350+685G>C ENSP00000374143.3:n.350+685G>C
ENST00000389494.7:c.373G>C ENSP00000374145.3:p.Ala125Pro
ENST00000485094.1:n.394G>C
NM_005199.4:c.373G>C NP_005190.4:p.Ala125Pro
NM_005199.5:c.373G>C MANE Select NP_005190.4:p.Ala125Pro
Search 100 bp 5'
Search 100 bp 3'