Canonical Allele Identifier: CA351008886
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233406158C>A (hg19) chr2:g.232541448C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541448C>A , CM000664.2:g.232541448C>A GRCh38
NC_000002.11:g.233406158C>A , CM000664.1:g.233406158C>A GRCh37
NC_000002.10:g.233114402C>A NCBI36
NG_012954.1:g.6722C>A
NG_012954.2:g.6757C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.425C>A MANE Select ENSP00000498757.1:p.Pro142Gln
ENST00000389492.3:c.350+737C>A ENSP00000374143.3:n.350+737C>A
ENST00000389494.7:c.425C>A ENSP00000374145.3:p.Pro142Gln
ENST00000485094.1:n.446C>A
NM_005199.4:c.425C>A NP_005190.4:p.Pro142Gln
NM_005199.5:c.425C>A MANE Select NP_005190.4:p.Pro142Gln
Search 100 bp 5'
Search 100 bp 3'