Canonical Allele Identifier: CA342629985
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543720G>C (hg19) chr1:g.154571244G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571244G>C , CM000663.2:g.154571244G>C GRCh38
NC_000001.10:g.154543720G>C , CM000663.1:g.154543720G>C GRCh37
NC_000001.9:g.152810344G>C NCBI36
NG_008027.1:g.8464G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.421G>C MANE Select ENSP00000357461.3:p.Gly141Arg
ENST00000636034.1:c.421G>C ENSP00000489703.1:p.Gly141Arg
ENST00000637900.1:c.427G>C ENSP00000490474.1:p.Gly143Arg
ENST00000368476.3:c.421G>C ENSP00000357461.3:p.Gly141Arg
NM_000748.2:c.421G>C NP_000739.1:p.Gly141Arg
XM_017000180.2:c.-9-81G>C XP_016855669.1:n.-9-81G>C
XR_001736952.2:n.673G>C
NM_000748.3:c.421G>C MANE Select NP_000739.1:p.Gly141Arg
Search 100 bp 5'
Search 100 bp 3'