Canonical Allele Identifier: CA1007940630
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs2149366076
gnomAD v3: 1-154569378-A-T
gnomAD v4: 1-154569378-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154569378A>T , CM000663.2:g.154569378A>T GRCh38
NC_000001.10:g.154541854A>T , CM000663.1:g.154541854A>T GRCh37
NC_000001.9:g.152808478A>T NCBI36
NG_008027.1:g.6598A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.65-84A>T MANE Select ENSP00000357461.3:n.65-84A>T
ENST00000636034.1:c.65-84A>T ENSP00000489703.1:n.65-84A>T
ENST00000637900.1:c.65-84A>T ENSP00000490474.1:n.65-84A>T
ENST00000368476.3:c.65-84A>T ENSP00000357461.3:n.65-84A>T
NM_000748.2:c.65-84A>T NP_000739.1:n.65-84A>T
XM_017000180.2:c.-310-84A>T XP_016855669.1:n.-310-84A>T
XR_001736952.2:n.317-84A>T
NM_000748.3:c.65-84A>T MANE Select NP_000739.1:n.65-84A>T
Search 100 bp 5'
Search 100 bp 3'