Canonical Allele Identifier: CA421230865

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154543788A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571312A>C , CM000663.2:g.154571312A>C	GRCh38
NC_000001.10:g.154543788A>C , CM000663.1:g.154543788A>C	GRCh37
NC_000001.9:g.152810412A>C	NCBI36
NG_008027.1:g.8532A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.489A>C MANE Select	ENSP00000357461.3:p.Pro163=
ENST00000636034.1:c.489A>C	ENSP00000489703.1:p.Pro163=
ENST00000637900.1:c.495A>C	ENSP00000490474.1:p.Pro165=
ENST00000368476.3:c.489A>C	ENSP00000357461.3:p.Pro163=
NM_000748.2:c.489A>C	NP_000739.1:p.Pro163=
XM_017000180.2:c.-9-13A>C	XP_016855669.1:n.-9-13A>C
XR_001736952.2:n.741A>C
NM_000748.3:c.489A>C MANE Select	NP_000739.1:p.Pro163=