Canonical Allele Identifier: CA351012026
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233407707G>C (hg19) chr2:g.232542997G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232542997G>C , CM000664.2:g.232542997G>C GRCh38
NC_000002.11:g.233407707G>C , CM000664.1:g.233407707G>C GRCh37
NC_000002.10:g.233115951G>C NCBI36
NG_012954.1:g.8271G>C
NG_012954.2:g.8306G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.720G>C MANE Select ENSP00000498757.1:p.Lys240Asn
ENST00000389492.3:c.564G>C ENSP00000374143.3:p.Lys188Asn
ENST00000389494.7:c.720G>C ENSP00000374145.3:p.Lys240Asn
NM_005199.4:c.720G>C NP_005190.4:p.Lys240Asn
NM_005199.5:c.720G>C MANE Select NP_005190.4:p.Lys240Asn
Search 100 bp 5'
Search 100 bp 3'