Canonical Allele Identifier: CA342630152
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1696160493
MyVariant Identifiers: chr1:g.154543792G>C (hg19) chr1:g.154571316G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571316G>C , CM000663.2:g.154571316G>C GRCh38
NC_000001.10:g.154543792G>C , CM000663.1:g.154543792G>C GRCh37
NC_000001.9:g.152810416G>C NCBI36
NG_008027.1:g.8536G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.493G>C MANE Select ENSP00000357461.3:p.Asp165His
ENST00000636034.1:c.493G>C ENSP00000489703.1:p.Asp165His
ENST00000637900.1:c.499G>C ENSP00000490474.1:p.Asp167His
ENST00000368476.3:c.493G>C ENSP00000357461.3:p.Asp165His
NM_000748.2:c.493G>C NP_000739.1:p.Asp165His
XM_017000180.2:c.-9-9G>C XP_016855669.1:n.-9-9G>C
XR_001736952.2:n.745G>C
NM_000748.3:c.493G>C MANE Select NP_000739.1:p.Asp165His
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