Canonical Allele Identifier: CA1335312282
Gene: CHRNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539980T= , CM000664.2:g.232539980T= GRCh38
NC_000002.11:g.233404690T= , CM000664.1:g.233404690T= GRCh37
NC_000002.10:g.233112934T= NCBI36
NG_012954.1:g.5254T=
NG_012954.2:g.5289T=

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.56-12T= MANE Select ENSP00000498757.1:n.56-12T=
ENST00000389492.3:c.56-12T= ENSP00000374143.3:n.56-12T=
ENST00000389494.7:c.56-12T= ENSP00000374145.3:n.56-12T=
ENST00000485094.1:n.77-12T=
NM_005199.4:c.56-12T= NP_005190.4:n.56-12T=
NM_005199.5:c.56-12T= MANE Select NP_005190.4:n.56-12T=
Search 100 bp 5'
Search 100 bp 3'