Canonical Allele Identifier: CA1167959208
Gene: BSND HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54999094T= , CM000663.2:g.54999094T= GRCh38
NC_000001.10:g.55464767T= , CM000663.1:g.55464767T= GRCh37
NC_000001.9:g.55237355T= NCBI36
NG_008965.1:g.5151T=
NG_008965.2:g.5162T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651561.1:c.-93T= MANE Select ENSP00000498282.1:n.-93T=
ENST00000371265.4:c.-93T= ENSP00000360312.4:n.-93T=
NM_057176.2:c.-93T= NP_476517.1:n.-93T=
NM_057176.3:c.-93T= MANE Select NP_476517.1:n.-93T=
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