Canonical Allele Identifier: CA351009202
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541490A>C , CM000664.2:g.232541490A>C GRCh38
NC_000002.11:g.233406200A>C , CM000664.1:g.233406200A>C GRCh37
NC_000002.10:g.233114444A>C NCBI36
NG_012954.1:g.6764A>C
NG_012954.2:g.6799A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.467A>C MANE Select ENSP00000498757.1:p.Tyr156Ser
ENST00000389492.3:c.350+779A>C ENSP00000374143.3:n.350+779A>C
ENST00000389494.7:c.467A>C ENSP00000374145.3:p.Tyr156Ser
ENST00000485094.1:n.488A>C
NM_005199.4:c.467A>C NP_005190.4:p.Tyr156Ser
NM_005199.5:c.467A>C MANE Select NP_005190.4:p.Tyr156Ser