Canonical Allele Identifier: CA2168757
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs765437470

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232542915C>A , CM000664.2:g.232542915C>A GRCh38
NC_000002.11:g.233407625C>A , CM000664.1:g.233407625C>A GRCh37
NC_000002.10:g.233115869C>A NCBI36
NG_012954.1:g.8189C>A
NG_012954.2:g.8224C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.638C>A MANE Select ENSP00000498757.1:p.Ala213Asp
ENST00000389492.3:c.482C>A ENSP00000374143.3:p.Ala161Asp
ENST00000389494.7:c.638C>A ENSP00000374145.3:p.Ala213Asp
NM_005199.4:c.638C>A NP_005190.4:p.Ala213Asp
NM_005199.5:c.638C>A MANE Select NP_005190.4:p.Ala213Asp