Canonical Allele Identifier: CA342630073
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs769929506
gnomAD v2: 1-154543759-G-T
gnomAD v3: 1-154571283-G-T
gnomAD v4: 1-154571283-G-T
MyVariant Identifiers: chr1:g.154543759G>T (hg19) chr1:g.154571283G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571283G>T , CM000663.2:g.154571283G>T GRCh38
NC_000001.10:g.154543759G>T , CM000663.1:g.154543759G>T GRCh37
NC_000001.9:g.152810383G>T NCBI36
NG_008027.1:g.8503G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.460G>T MANE Select ENSP00000357461.3:p.Ala154Ser
ENST00000636034.1:c.460G>T ENSP00000489703.1:p.Ala154Ser
ENST00000637900.1:c.466G>T ENSP00000490474.1:p.Ala156Ser
ENST00000368476.3:c.460G>T ENSP00000357461.3:p.Ala154Ser
NM_000748.2:c.460G>T NP_000739.1:p.Ala154Ser
XM_017000180.2:c.-9-42G>T XP_016855669.1:n.-9-42G>T
XR_001736952.2:n.712G>T
NM_000748.3:c.460G>T MANE Select NP_000739.1:p.Ala154Ser
Search 100 bp 5'
Search 100 bp 3'