Canonical Allele Identifier: CA351008911
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233406163G>C (hg19) chr2:g.232541453G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541453G>C , CM000664.2:g.232541453G>C GRCh38
NC_000002.11:g.233406163G>C , CM000664.1:g.233406163G>C GRCh37
NC_000002.10:g.233114407G>C NCBI36
NG_012954.1:g.6727G>C
NG_012954.2:g.6762G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.430G>C MANE Select ENSP00000498757.1:p.Ala144Pro
ENST00000389492.3:c.350+742G>C ENSP00000374143.3:n.350+742G>C
ENST00000389494.7:c.430G>C ENSP00000374145.3:p.Ala144Pro
ENST00000485094.1:n.451G>C
NM_005199.4:c.430G>C NP_005190.4:p.Ala144Pro
NM_005199.5:c.430G>C MANE Select NP_005190.4:p.Ala144Pro
Search 100 bp 5'
Search 100 bp 3'