Canonical Allele Identifier: CA351006772
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233404489T>G (hg19) chr2:g.232539779T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539779T>G , CM000664.2:g.232539779T>G GRCh38
NC_000002.11:g.233404489T>G , CM000664.1:g.233404489T>G GRCh37
NC_000002.10:g.233112733T>G NCBI36
NG_012954.1:g.5053T>G
NG_012954.2:g.5088T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.32T>G MANE Select ENSP00000498757.1:p.Leu11Arg
ENST00000389492.3:c.32T>G ENSP00000374143.3:p.Leu11Arg
ENST00000389494.7:c.32T>G ENSP00000374145.3:p.Leu11Arg
ENST00000485094.1:n.53T>G
NM_005199.4:c.32T>G NP_005190.4:p.Leu11Arg
NM_005199.5:c.32T>G MANE Select NP_005190.4:p.Leu11Arg
Search 100 bp 5'
Search 100 bp 3'