Canonical Allele Identifier: CA766144511
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs1429988642
MyVariant Identifiers: chr2:g.233407896A>C (hg19) chr2:g.232543186A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543186A>C , CM000664.2:g.232543186A>C GRCh38
NC_000002.11:g.233407896A>C , CM000664.1:g.233407896A>C GRCh37
NC_000002.10:g.233116140A>C NCBI36
NG_012954.1:g.8460A>C
NG_012954.2:g.8495A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.806-89A>C MANE Select ENSP00000498757.1:n.806-89A>C
ENST00000389492.3:c.650-89A>C ENSP00000374143.3:n.650-89A>C
ENST00000389494.7:c.806-89A>C ENSP00000374145.3:n.806-89A>C
NM_005199.4:c.806-89A>C NP_005190.4:n.806-89A>C
NM_005199.5:c.806-89A>C MANE Select NP_005190.4:n.806-89A>C
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