Canonical Allele Identifier: CA1130708
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs763576683
ExAC: 1:154543628 G / C
gnomAD v2: 1-154543628-G-C
gnomAD v3: 1-154571152-G-C
gnomAD v4: 1-154571152-G-C
MyVariant Identifiers: chr1:g.154543628G>C (hg19) chr1:g.154571152G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571152G>C , CM000663.2:g.154571152G>C GRCh38
NC_000001.10:g.154543628G>C , CM000663.1:g.154543628G>C GRCh37
NC_000001.9:g.152810252G>C NCBI36
NG_008027.1:g.8372G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.366-37G>C MANE Select ENSP00000357461.3:n.366-37G>C
ENST00000636034.1:c.366-37G>C ENSP00000489703.1:n.366-37G>C
ENST00000637900.1:c.372-37G>C ENSP00000490474.1:n.372-37G>C
ENST00000368476.3:c.366-37G>C ENSP00000357461.3:n.366-37G>C
NM_000748.2:c.366-37G>C NP_000739.1:n.366-37G>C
XM_017000180.2:c.-9-173G>C XP_016855669.1:n.-9-173G>C
XR_001736952.2:n.618-37G>C
NM_000748.3:c.366-37G>C MANE Select NP_000739.1:n.366-37G>C
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