Canonical Allele Identifier: CA1335317509
Gene: CHRNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232542970G= , CM000664.2:g.232542970G= GRCh38
NC_000002.11:g.233407680G= , CM000664.1:g.233407680G= GRCh37
NC_000002.10:g.233115924G= NCBI36
NG_012954.1:g.8244G=
NG_012954.2:g.8279G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.693G= MANE Select ENSP00000498757.1:p.Val231=
ENST00000389492.3:c.537G= ENSP00000374143.3:p.Val179=
ENST00000389494.7:c.693G= ENSP00000374145.3:p.Val231=
NM_005199.4:c.693G= NP_005190.4:p.Val231=
NM_005199.5:c.693G= MANE Select NP_005190.4:p.Val231=
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