Canonical Allele Identifier: CA2648171644
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154569383-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154569383C>T , CM000663.2:g.154569383C>T GRCh38
NC_000001.10:g.154541859C>T , CM000663.1:g.154541859C>T GRCh37
NC_000001.9:g.152808483C>T NCBI36
NG_008027.1:g.6603C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.65-79C>T MANE Select ENSP00000357461.3:n.65-79C>T
ENST00000636034.1:c.65-79C>T ENSP00000489703.1:n.65-79C>T
ENST00000637900.1:c.65-79C>T ENSP00000490474.1:n.65-79C>T
ENST00000368476.3:c.65-79C>T ENSP00000357461.3:n.65-79C>T
NM_000748.2:c.65-79C>T NP_000739.1:n.65-79C>T
XM_017000180.2:c.-310-79C>T XP_016855669.1:n.-310-79C>T
XR_001736952.2:n.317-79C>T
NM_000748.3:c.65-79C>T MANE Select NP_000739.1:n.65-79C>T
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