Canonical Allele Identifier: CA2635846292

Gene: CHRNB1

Linked Data

• gnomAD v4: 17-7454561-C-CCATAGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454561_7454562insCATAGGG , CM000679.2:g.7454561_7454562insCATAGGG	GRCh38
NC_000017.10:g.7357880_7357881insCATAGGG , CM000679.1:g.7357880_7357881insCATAGGG	GRCh37
NC_000017.9:g.7298604_7298605insCATAGGG	NCBI36
NG_008026.1:g.14475_14476insCATAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1044+41_1044+42insCATAGGG MANE Select	ENSP00000304290.2:n.1044+41_1044+42insCATAGGG
ENST00000306071.6:c.1044+41_1044+42insCATAGGG	ENSP00000304290.2:n.1044+41_1044+42insCATAGGG
ENST00000536404.6:c.828+41_828+42insCATAGGG	ENSP00000439209.2:n.828+41_828+42insCATAGGG
ENST00000570557.5:c.707+41_707+42insCATAGGG
ENST00000573209.1:n.1988+41_1988+42insCATAGGG
ENST00000576360.1:c.681+41_681+42insCATAGGG	ENSP00000459092.1:n.681+41_681+42insCATAGGG
NM_000747.2:c.1044+41_1044+42insCATAGGG	NP_000738.2:n.1044+41_1044+42insCATAGGG
NM_000747.3:c.1044+41_1044+42insCATAGGG MANE Select	NP_000738.2:n.1044+41_1044+42insCATAGGG