Canonical Allele Identifier: CA421231129
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543917G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571441G>C , CM000663.2:g.154571441G>C GRCh38
NC_000001.10:g.154543917G>C , CM000663.1:g.154543917G>C GRCh37
NC_000001.9:g.152810541G>C NCBI36
NG_008027.1:g.8661G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.618G>C MANE Select ENSP00000357461.3:p.Val206=
ENST00000636034.1:c.618G>C ENSP00000489703.1:p.Val206=
ENST00000637900.1:c.624G>C ENSP00000490474.1:p.Val208=
ENST00000368476.3:c.618G>C ENSP00000357461.3:p.Val206=
NM_000748.2:c.618G>C NP_000739.1:p.Val206=
XM_017000180.2:c.108G>C XP_016855669.1:p.Val36=
XR_001736952.2:n.870G>C
NM_000748.3:c.618G>C MANE Select NP_000739.1:p.Val206=