Canonical Allele Identifier: CA2577278048

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232539881T>C , CM000664.2:g.232539881T>C	GRCh38
NC_000002.11:g.233404591T>C , CM000664.1:g.233404591T>C	GRCh37
NC_000002.10:g.233112835T>C	NCBI36
NG_012954.1:g.5155T>C
NG_012954.2:g.5190T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.55+79T>C MANE Select	ENSP00000498757.1:n.55+79T>C
ENST00000389492.3:c.55+79T>C	ENSP00000374143.3:n.55+79T>C
ENST00000389494.7:c.55+79T>C	ENSP00000374145.3:n.55+79T>C
ENST00000485094.1:n.76+79T>C
NM_005199.4:c.55+79T>C	NP_005190.4:n.55+79T>C
NM_005199.5:c.55+79T>C MANE Select	NP_005190.4:n.55+79T>C