Canonical Allele Identifier: CA342629885
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571197G>T , CM000663.2:g.154571197G>T GRCh38
NC_000001.10:g.154543673G>T , CM000663.1:g.154543673G>T GRCh37
NC_000001.9:g.152810297G>T NCBI36
NG_008027.1:g.8417G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.374G>T MANE Select ENSP00000357461.3:p.Gly125Val
ENST00000636034.1:c.374G>T ENSP00000489703.1:p.Gly125Val
ENST00000637900.1:c.380G>T ENSP00000490474.1:p.Gly127Val
ENST00000368476.3:c.374G>T ENSP00000357461.3:p.Gly125Val
NM_000748.2:c.374G>T NP_000739.1:p.Gly125Val
XM_017000180.2:c.-9-128G>T XP_016855669.1:n.-9-128G>T
XR_001736952.2:n.626G>T
NM_000748.3:c.374G>T MANE Select NP_000739.1:p.Gly125Val