Canonical Allele Identifier: CA342629862
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543664G>A (hg19) chr1:g.154571188G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571188G>A , CM000663.2:g.154571188G>A GRCh38
NC_000001.10:g.154543664G>A , CM000663.1:g.154543664G>A GRCh37
NC_000001.9:g.152810288G>A NCBI36
NG_008027.1:g.8408G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.366-1G>A MANE Select ENSP00000357461.3:n.366-1G>A
ENST00000636034.1:c.366-1G>A ENSP00000489703.1:n.366-1G>A
ENST00000637900.1:c.372-1G>A ENSP00000490474.1:n.372-1G>A
ENST00000368476.3:c.366-1G>A ENSP00000357461.3:n.366-1G>A
NM_000748.2:c.366-1G>A NP_000739.1:n.366-1G>A
XM_017000180.2:c.-9-137G>A XP_016855669.1:n.-9-137G>A
XR_001736952.2:n.618-1G>A
NM_000748.3:c.366-1G>A MANE Select NP_000739.1:n.366-1G>A
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