Canonical Allele Identifier: CA351012061
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233407712T>G (hg19) chr2:g.232543002T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543002T>G , CM000664.2:g.232543002T>G GRCh38
NC_000002.11:g.233407712T>G , CM000664.1:g.233407712T>G GRCh37
NC_000002.10:g.233115956T>G NCBI36
NG_012954.1:g.8276T>G
NG_012954.2:g.8311T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.725T>G MANE Select ENSP00000498757.1:p.Leu242Arg
ENST00000389492.3:c.569T>G ENSP00000374143.3:p.Leu190Arg
ENST00000389494.7:c.725T>G ENSP00000374145.3:p.Leu242Arg
NM_005199.4:c.725T>G NP_005190.4:p.Leu242Arg
NM_005199.5:c.725T>G MANE Select NP_005190.4:p.Leu242Arg
Search 100 bp 5'
Search 100 bp 3'