Canonical Allele Identifier: CA342629859

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154543663A>C (hg19) ; chr1:g.154571187A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571187A>C , CM000663.2:g.154571187A>C	GRCh38
NC_000001.10:g.154543663A>C , CM000663.1:g.154543663A>C	GRCh37
NC_000001.9:g.152810287A>C	NCBI36
NG_008027.1:g.8407A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.366-2A>C MANE Select	ENSP00000357461.3:n.366-2A>C
ENST00000636034.1:c.366-2A>C	ENSP00000489703.1:n.366-2A>C
ENST00000637900.1:c.372-2A>C	ENSP00000490474.1:n.372-2A>C
ENST00000368476.3:c.366-2A>C	ENSP00000357461.3:n.366-2A>C
NM_000748.2:c.366-2A>C	NP_000739.1:n.366-2A>C
XM_017000180.2:c.-9-138A>C	XP_016855669.1:n.-9-138A>C
XR_001736952.2:n.618-2A>C
NM_000748.3:c.366-2A>C MANE Select	NP_000739.1:n.366-2A>C