Canonical Allele Identifier: CA351011813

Gene: CHRNG

Linked Data

• MyVariant Identifiers: chr2:g.233407676A>T (hg19) ; chr2:g.232542966A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232542966A>T , CM000664.2:g.232542966A>T	GRCh38
NC_000002.11:g.233407676A>T , CM000664.1:g.233407676A>T	GRCh37
NC_000002.10:g.233115920A>T	NCBI36
NG_012954.1:g.8240A>T
NG_012954.2:g.8275A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.689A>T MANE Select	ENSP00000498757.1:p.Lys230Met
ENST00000389492.3:c.533A>T	ENSP00000374143.3:p.Lys178Met
ENST00000389494.7:c.689A>T	ENSP00000374145.3:p.Lys230Met
NM_005199.4:c.689A>T	NP_005190.4:p.Lys230Met
NM_005199.5:c.689A>T MANE Select	NP_005190.4:p.Lys230Met