Canonical Allele Identifier: CA342630091

Gene: CHRNB2

Linked Data

• gnomAD v4: 1-154571291-G-C
• COSMIC: COSM6121526
• MyVariant Identifiers: chr1:g.154543767G>C (hg19) ; chr1:g.154571291G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571291G>C , CM000663.2:g.154571291G>C	GRCh38
NC_000001.10:g.154543767G>C , CM000663.1:g.154543767G>C	GRCh37
NC_000001.9:g.152810391G>C	NCBI36
NG_008027.1:g.8511G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.468G>C MANE Select	ENSP00000357461.3:p.Lys156Asn
ENST00000636034.1:c.468G>C	ENSP00000489703.1:p.Lys156Asn
ENST00000637900.1:c.474G>C	ENSP00000490474.1:p.Lys158Asn
ENST00000368476.3:c.468G>C	ENSP00000357461.3:p.Lys156Asn
NM_000748.2:c.468G>C	NP_000739.1:p.Lys156Asn
XM_017000180.2:c.-9-34G>C	XP_016855669.1:n.-9-34G>C
XR_001736952.2:n.720G>C
NM_000748.3:c.468G>C MANE Select	NP_000739.1:p.Lys156Asn