Canonical Allele Identifier: CA2635847041

Gene: CHRNB1

Linked Data

• gnomAD v4: 17-7455992-ACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455996_7455997del , CM000679.2:g.7455996_7455997del	GRCh38
NC_000017.10:g.7359315_7359316del , CM000679.1:g.7359315_7359316del	GRCh37
NC_000017.9:g.7300039_7300040del	NCBI36
NG_008026.1:g.15910_15911del

Transcript Alleles

HGVS	Amino-acid change
ENST00000306071.7:c.1365+55_1365+56del MANE Select	ENSP00000304290.2:n.1365+55_1365+56del
ENST00000306071.6:c.1365+55_1365+56del	ENSP00000304290.2:n.1365+55_1365+56del
ENST00000536404.6:c.1149+55_1149+56del	ENSP00000439209.2:n.1149+55_1149+56del
ENST00000575379.1:c.-28+55_-28+56del	ENSP00000461751.1:n.-28+55_-28+56del
ENST00000576360.1:c.1002+55_1002+56del	ENSP00000459092.1:n.1002+55_1002+56del
NM_000747.2:c.1365+55_1365+56del	NP_000738.2:n.1365+55_1365+56del
NM_000747.3:c.1365+55_1365+56del MANE Select	NP_000738.2:n.1365+55_1365+56del