Canonical Allele Identifier: CA1167959262
Gene: BSND HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54999222T= , CM000663.2:g.54999222T= GRCh38
NC_000001.10:g.55464895T= , CM000663.1:g.55464895T= GRCh37
NC_000001.9:g.55237483T= NCBI36
NG_008965.1:g.5279T=
NG_008965.2:g.5290T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651561.1:c.36T= MANE Select ENSP00000498282.1:p.Ile12=
ENST00000371265.4:c.36T= ENSP00000360312.4:p.Ile12=
NM_057176.2:c.36T= NP_476517.1:p.Ile12=
NM_057176.3:c.36T= MANE Select NP_476517.1:p.Ile12=
Search 100 bp 5'
Search 100 bp 3'