Canonical Allele Identifier: CA889604089

Gene: CHRNB2

Linked Data

• dbSNP Id: rs1223752792
• gnomAD v3: 1-154576249-C-G
• gnomAD v4: 1-154576249-C-G
• MyVariant Identifiers: chr1:g.154548725C>G (hg19) ; chr1:g.154576249C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154576249C>G , CM000663.2:g.154576249C>G	GRCh38
NC_000001.10:g.154548725C>G , CM000663.1:g.154548725C>G	GRCh37
NC_000001.9:g.152815349C>G	NCBI36
NG_008027.1:g.13469C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368476.4:c.*317C>G MANE Select	ENSP00000357461.3:n.*317C>G
ENST00000636034.1:c.1505+321C>G	ENSP00000489703.1:n.1505+321C>G
ENST00000637900.1:c.*317C>G	ENSP00000490474.1:n.*317C>G
ENST00000368476.3:c.*317C>G	ENSP00000357461.3:n.*317C>G
NM_000748.2:c.*317C>G	NP_000739.1:n.*317C>G
XM_017000180.2:c.*317C>G	XP_016855669.1:n.*317C>G
XR_001736952.2:n.2078C>G
NM_000748.3:c.*317C>G MANE Select	NP_000739.1:n.*317C>G