Canonical Allele Identifier: CA351009232
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233406204C>G (hg19) chr2:g.232541494C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541494C>G , CM000664.2:g.232541494C>G GRCh38
NC_000002.11:g.233406204C>G , CM000664.1:g.233406204C>G GRCh37
NC_000002.10:g.233114448C>G NCBI36
NG_012954.1:g.6768C>G
NG_012954.2:g.6803C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.471C>G MANE Select ENSP00000498757.1:p.Phe157Leu
ENST00000389492.3:c.350+783C>G ENSP00000374143.3:n.350+783C>G
ENST00000389494.7:c.471C>G ENSP00000374145.3:p.Phe157Leu
ENST00000485094.1:n.492C>G
NM_005199.4:c.471C>G NP_005190.4:p.Phe157Leu
NM_005199.5:c.471C>G MANE Select NP_005190.4:p.Phe157Leu
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