Canonical Allele Identifier: CA1335312190
Gene: CHRNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539809C= , CM000664.2:g.232539809C= GRCh38
NC_000002.11:g.233404519C= , CM000664.1:g.233404519C= GRCh37
NC_000002.10:g.233112763C= NCBI36
NG_012954.1:g.5083C=
NG_012954.2:g.5118C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.55+7C= MANE Select ENSP00000498757.1:n.55+7C=
ENST00000389492.3:c.55+7C= ENSP00000374143.3:n.55+7C=
ENST00000389494.7:c.55+7C= ENSP00000374145.3:n.55+7C=
ENST00000485094.1:n.76+7C=
NM_005199.4:c.55+7C= NP_005190.4:n.55+7C=
NM_005199.5:c.55+7C= MANE Select NP_005190.4:n.55+7C=