Canonical Allele Identifier: CA342630418
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543887C>G (hg19) chr1:g.154571411C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571411C>G , CM000663.2:g.154571411C>G GRCh38
NC_000001.10:g.154543887C>G , CM000663.1:g.154543887C>G GRCh37
NC_000001.9:g.152810511C>G NCBI36
NG_008027.1:g.8631C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.588C>G MANE Select ENSP00000357461.3:p.Asp196Glu
ENST00000636034.1:c.588C>G ENSP00000489703.1:p.Asp196Glu
ENST00000637900.1:c.594C>G ENSP00000490474.1:p.Asp198Glu
ENST00000368476.3:c.588C>G ENSP00000357461.3:p.Asp196Glu
NM_000748.2:c.588C>G NP_000739.1:p.Asp196Glu
XM_017000180.2:c.78C>G XP_016855669.1:p.Asp26Glu
XR_001736952.2:n.840C>G
NM_000748.3:c.588C>G MANE Select NP_000739.1:p.Asp196Glu
Search 100 bp 5'
Search 100 bp 3'