Canonical Allele Identifier: CA351008935
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs1574643994
MyVariant Identifiers: chr2:g.233406166A>T (hg19) chr2:g.232541456A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541456A>T , CM000664.2:g.232541456A>T GRCh38
NC_000002.11:g.233406166A>T , CM000664.1:g.233406166A>T GRCh37
NC_000002.10:g.233114410A>T NCBI36
NG_012954.1:g.6730A>T
NG_012954.2:g.6765A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.433A>T MANE Select ENSP00000498757.1:p.Ile145Phe
ENST00000389492.3:c.350+745A>T ENSP00000374143.3:n.350+745A>T
ENST00000389494.7:c.433A>T ENSP00000374145.3:p.Ile145Phe
ENST00000485094.1:n.454A>T
NM_005199.4:c.433A>T NP_005190.4:p.Ile145Phe
NM_005199.5:c.433A>T MANE Select NP_005190.4:p.Ile145Phe
Search 100 bp 5'
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