Canonical Allele Identifier: CA1335312252
Gene: CHRNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539943G= , CM000664.2:g.232539943G= GRCh38
NC_000002.11:g.233404653G= , CM000664.1:g.233404653G= GRCh37
NC_000002.10:g.233112897G= NCBI36
NG_012954.1:g.5217G=
NG_012954.2:g.5252G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.56-49G= MANE Select ENSP00000498757.1:n.56-49G=
ENST00000389492.3:c.56-49G= ENSP00000374143.3:n.56-49G=
ENST00000389494.7:c.56-49G= ENSP00000374145.3:n.56-49G=
ENST00000485094.1:n.77-49G=
NM_005199.4:c.56-49G= NP_005190.4:n.56-49G=
NM_005199.5:c.56-49G= MANE Select NP_005190.4:n.56-49G=
Search 100 bp 5'
Search 100 bp 3'