Canonical Allele Identifier: CA1335316783
Gene: CHRNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541517C= , CM000664.2:g.232541517C= GRCh38
NC_000002.11:g.233406227C= , CM000664.1:g.233406227C= GRCh37
NC_000002.10:g.233114471C= NCBI36
NG_012954.1:g.6791C=
NG_012954.2:g.6826C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.494C= MANE Select ENSP00000498757.1:p.Ser165=
ENST00000389492.3:c.350+806C= ENSP00000374143.3:n.350+806C=
ENST00000389494.7:c.494C= ENSP00000374145.3:p.Ser165=
ENST00000485094.1:n.515C=
NM_005199.4:c.494C= NP_005190.4:p.Ser165=
NM_005199.5:c.494C= MANE Select NP_005190.4:p.Ser165=