Canonical Allele Identifier: CA417956584
Gene: BSND HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.55464955G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54999282G>A , CM000663.2:g.54999282G>A GRCh38
NC_000001.10:g.55464955G>A , CM000663.1:g.55464955G>A GRCh37
NC_000001.9:g.55237543G>A NCBI36
NG_008965.1:g.5339G>A
NG_008965.2:g.5350G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651561.1:c.96G>A MANE Select ENSP00000498282.1:p.Gln32=
ENST00000371265.4:c.96G>A ENSP00000360312.4:p.Gln32=
NM_057176.2:c.96G>A NP_476517.1:p.Gln32=
NM_057176.3:c.96G>A MANE Select NP_476517.1:p.Gln32=
Search 100 bp 5'
Search 100 bp 3'