Canonical Allele Identifier: CA351012021
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233407706A>G (hg19) chr2:g.232542996A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232542996A>G , CM000664.2:g.232542996A>G GRCh38
NC_000002.11:g.233407706A>G , CM000664.1:g.233407706A>G GRCh37
NC_000002.10:g.233115950A>G NCBI36
NG_012954.1:g.8270A>G
NG_012954.2:g.8305A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.719A>G MANE Select ENSP00000498757.1:p.Lys240Arg
ENST00000389492.3:c.563A>G ENSP00000374143.3:p.Lys188Arg
ENST00000389494.7:c.719A>G ENSP00000374145.3:p.Lys240Arg
NM_005199.4:c.719A>G NP_005190.4:p.Lys240Arg
NM_005199.5:c.719A>G MANE Select NP_005190.4:p.Lys240Arg
Search 100 bp 5'
Search 100 bp 3'