Canonical Allele Identifier: CA351006932
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232540043A>T , CM000664.2:g.232540043A>T GRCh38
NC_000002.11:g.233404753A>T , CM000664.1:g.233404753A>T GRCh37
NC_000002.10:g.233112997A>T NCBI36
NG_012954.1:g.5317A>T
NG_012954.2:g.5352A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.107A>T MANE Select ENSP00000498757.1:p.Asn36Ile
ENST00000389492.3:c.107A>T ENSP00000374143.3:p.Asn36Ile
ENST00000389494.7:c.107A>T ENSP00000374145.3:p.Asn36Ile
ENST00000485094.1:n.128A>T
NM_005199.4:c.107A>T NP_005190.4:p.Asn36Ile
NM_005199.5:c.107A>T MANE Select NP_005190.4:p.Asn36Ile