Canonical Allele Identifier: CA2754657284
Gene: CHRNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539916C>T , CM000664.2:g.232539916C>T GRCh38
NC_000002.11:g.233404626C>T , CM000664.1:g.233404626C>T GRCh37
NC_000002.10:g.233112870C>T NCBI36
NG_012954.1:g.5190C>T
NG_012954.2:g.5225C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.56-76C>T MANE Select ENSP00000498757.1:n.56-76C>T
ENST00000389492.3:c.56-76C>T ENSP00000374143.3:n.56-76C>T
ENST00000389494.7:c.56-76C>T ENSP00000374145.3:n.56-76C>T
ENST00000485094.1:n.77-76C>T
NM_005199.4:c.56-76C>T NP_005190.4:n.56-76C>T
NM_005199.5:c.56-76C>T MANE Select NP_005190.4:n.56-76C>T
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