Canonical Allele Identifier: CA2635847029

Gene: CHRNB1

Linked Data

• gnomAD v4: 17-7455987-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455991del , CM000679.2:g.7455991del	GRCh38
NC_000017.10:g.7359310del , CM000679.1:g.7359310del	GRCh37
NC_000017.9:g.7300034del	NCBI36
NG_008026.1:g.15905del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1365+50del MANE Select	ENSP00000304290.2:n.1365+50del
ENST00000306071.6:c.1365+50del	ENSP00000304290.2:n.1365+50del
ENST00000536404.6:c.1149+50del	ENSP00000439209.2:n.1149+50del
ENST00000575379.1:c.-28+50del	ENSP00000461751.1:n.-28+50del
ENST00000576360.1:c.1002+50del	ENSP00000459092.1:n.1002+50del
NM_000747.2:c.1365+50del	NP_000738.2:n.1365+50del
NM_000747.3:c.1365+50del MANE Select	NP_000738.2:n.1365+50del