Canonical Allele Identifier: CA351011980
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233407702C>A (hg19) chr2:g.232542992C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232542992C>A , CM000664.2:g.232542992C>A GRCh38
NC_000002.11:g.233407702C>A , CM000664.1:g.233407702C>A GRCh37
NC_000002.10:g.233115946C>A NCBI36
NG_012954.1:g.8266C>A
NG_012954.2:g.8301C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.715C>A MANE Select ENSP00000498757.1:p.Arg239Ser
ENST00000389492.3:c.559C>A ENSP00000374143.3:p.Arg187Ser
ENST00000389494.7:c.715C>A ENSP00000374145.3:p.Arg239Ser
NM_005199.4:c.715C>A NP_005190.4:p.Arg239Ser
NM_005199.5:c.715C>A MANE Select NP_005190.4:p.Arg239Ser
Search 100 bp 5'
Search 100 bp 3'