Canonical Allele Identifier: CA342629871
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543667C>G (hg19) chr1:g.154571191C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571191C>G , CM000663.2:g.154571191C>G GRCh38
NC_000001.10:g.154543667C>G , CM000663.1:g.154543667C>G GRCh37
NC_000001.9:g.152810291C>G NCBI36
NG_008027.1:g.8411C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.368C>G MANE Select ENSP00000357461.3:p.Ala123Gly
ENST00000636034.1:c.368C>G ENSP00000489703.1:p.Ala123Gly
ENST00000637900.1:c.374C>G ENSP00000490474.1:p.Ala125Gly
ENST00000368476.3:c.368C>G ENSP00000357461.3:p.Ala123Gly
NM_000748.2:c.368C>G NP_000739.1:p.Ala123Gly
XM_017000180.2:c.-9-134C>G XP_016855669.1:n.-9-134C>G
XR_001736952.2:n.620C>G
NM_000748.3:c.368C>G MANE Select NP_000739.1:p.Ala123Gly
Search 100 bp 5'
Search 100 bp 3'