Canonical Allele Identifier: CA342629873
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154571193-G-A
MyVariant Identifiers: chr1:g.154543669G>A (hg19) chr1:g.154571193G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571193G>A , CM000663.2:g.154571193G>A GRCh38
NC_000001.10:g.154543669G>A , CM000663.1:g.154543669G>A GRCh37
NC_000001.9:g.152810293G>A NCBI36
NG_008027.1:g.8413G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.370G>A MANE Select ENSP00000357461.3:p.Asp124Asn
ENST00000636034.1:c.370G>A ENSP00000489703.1:p.Asp124Asn
ENST00000637900.1:c.376G>A ENSP00000490474.1:p.Asp126Asn
ENST00000368476.3:c.370G>A ENSP00000357461.3:p.Asp124Asn
NM_000748.2:c.370G>A NP_000739.1:p.Asp124Asn
XM_017000180.2:c.-9-132G>A XP_016855669.1:n.-9-132G>A
XR_001736952.2:n.622G>A
NM_000748.3:c.370G>A MANE Select NP_000739.1:p.Asp124Asn
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