Canonical Allele Identifier: CA1335316675
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs1574643860

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541322T>G , CM000664.2:g.232541322T>G GRCh38
NC_000002.11:g.233406032T>G , CM000664.1:g.233406032T>G GRCh37
NC_000002.10:g.233114276T>G NCBI36
NG_012954.1:g.6596T>G
NG_012954.2:g.6631T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.351-52T>G MANE Select ENSP00000498757.1:n.351-52T>G
ENST00000389492.3:c.350+611T>G ENSP00000374143.3:n.350+611T>G
ENST00000389494.7:c.351-52T>G ENSP00000374145.3:n.351-52T>G
ENST00000485094.1:n.372-52T>G
NM_005199.4:c.351-52T>G NP_005190.4:n.351-52T>G
NM_005199.5:c.351-52T>G MANE Select NP_005190.4:n.351-52T>G