Canonical Allele Identifier: CA417956514
Gene: BSND HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.55464889C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54999216C>A , CM000663.2:g.54999216C>A GRCh38
NC_000001.10:g.55464889C>A , CM000663.1:g.55464889C>A GRCh37
NC_000001.9:g.55237477C>A NCBI36
NG_008965.1:g.5273C>A
NG_008965.2:g.5284C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651561.1:c.30C>A MANE Select ENSP00000498282.1:p.Gly10=
ENST00000371265.4:c.30C>A ENSP00000360312.4:p.Gly10=
NM_057176.2:c.30C>A NP_476517.1:p.Gly10=
NM_057176.3:c.30C>A MANE Select NP_476517.1:p.Gly10=
Search 100 bp 5'
Search 100 bp 3'