Canonical Allele Identifier: CA342630483
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571440T>G , CM000663.2:g.154571440T>G GRCh38
NC_000001.10:g.154543916T>G , CM000663.1:g.154543916T>G GRCh37
NC_000001.9:g.152810540T>G NCBI36
NG_008027.1:g.8660T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.617T>G MANE Select ENSP00000357461.3:p.Val206Gly
ENST00000636034.1:c.617T>G ENSP00000489703.1:p.Val206Gly
ENST00000637900.1:c.623T>G ENSP00000490474.1:p.Val208Gly
ENST00000368476.3:c.617T>G ENSP00000357461.3:p.Val206Gly
NM_000748.2:c.617T>G NP_000739.1:p.Val206Gly
XM_017000180.2:c.107T>G XP_016855669.1:p.Val36Gly
XR_001736952.2:n.869T>G
NM_000748.3:c.617T>G MANE Select NP_000739.1:p.Val206Gly