Canonical Allele Identifier: CA1167959271
Gene: BSND HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54999258C= , CM000663.2:g.54999258C= GRCh38
NC_000001.10:g.55464931C= , CM000663.1:g.55464931C= GRCh37
NC_000001.9:g.55237519C= NCBI36
NG_008965.1:g.5315C=
NG_008965.2:g.5326C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651561.1:c.72C= MANE Select ENSP00000498282.1:p.Phe24=
ENST00000371265.4:c.72C= ENSP00000360312.4:p.Phe24=
NM_057176.2:c.72C= NP_476517.1:p.Phe24=
NM_057176.3:c.72C= MANE Select NP_476517.1:p.Phe24=
Search 100 bp 5'
Search 100 bp 3'