Canonical Allele Identifier: CA889603922
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1424786333
gnomAD v3: 1-154576121-G-A
gnomAD v4: 1-154576121-G-A
MyVariant Identifiers: chr1:g.154548597G>A (hg19) chr1:g.154576121G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576121G>A , CM000663.2:g.154576121G>A GRCh38
NC_000001.10:g.154548597G>A , CM000663.1:g.154548597G>A GRCh37
NC_000001.9:g.152815221G>A NCBI36
NG_008027.1:g.13341G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*189G>A MANE Select ENSP00000357461.3:n.*189G>A
ENST00000636034.1:c.1505+193G>A ENSP00000489703.1:n.1505+193G>A
ENST00000637900.1:c.*189G>A ENSP00000490474.1:n.*189G>A
ENST00000368476.3:c.*189G>A ENSP00000357461.3:n.*189G>A
NM_000748.2:c.*189G>A NP_000739.1:n.*189G>A
XM_017000180.2:c.*189G>A XP_016855669.1:n.*189G>A
XR_001736952.2:n.1950G>A
NM_000748.3:c.*189G>A MANE Select NP_000739.1:n.*189G>A
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