Canonical Allele Identifier: CA30837813
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1052997239
gnomAD v4: 1-154576187-G-A
MyVariant Identifiers: chr1:g.154548663G>A (hg19) chr1:g.154576187G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576187G>A , CM000663.2:g.154576187G>A GRCh38
NC_000001.10:g.154548663G>A , CM000663.1:g.154548663G>A GRCh37
NC_000001.9:g.152815287G>A NCBI36
NG_008027.1:g.13407G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*255G>A MANE Select ENSP00000357461.3:n.*255G>A
ENST00000636034.1:c.1505+259G>A ENSP00000489703.1:n.1505+259G>A
ENST00000637900.1:c.*255G>A ENSP00000490474.1:n.*255G>A
ENST00000368476.3:c.*255G>A ENSP00000357461.3:n.*255G>A
NM_000748.2:c.*255G>A NP_000739.1:n.*255G>A
XM_017000180.2:c.*255G>A XP_016855669.1:n.*255G>A
XR_001736952.2:n.2016G>A
NM_000748.3:c.*255G>A MANE Select NP_000739.1:n.*255G>A
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