Canonical Allele Identifier: CA351009151
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233406193G>T (hg19) chr2:g.232541483G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541483G>T , CM000664.2:g.232541483G>T GRCh38
NC_000002.11:g.233406193G>T , CM000664.1:g.233406193G>T GRCh37
NC_000002.10:g.233114437G>T NCBI36
NG_012954.1:g.6757G>T
NG_012954.2:g.6792G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.460G>T MANE Select ENSP00000498757.1:p.Val154Phe
ENST00000389492.3:c.350+772G>T ENSP00000374143.3:n.350+772G>T
ENST00000389494.7:c.460G>T ENSP00000374145.3:p.Val154Phe
ENST00000485094.1:n.481G>T
NM_005199.4:c.460G>T NP_005190.4:p.Val154Phe
NM_005199.5:c.460G>T MANE Select NP_005190.4:p.Val154Phe
Search 100 bp 5'
Search 100 bp 3'