Canonical Allele Identifier: CA1167959249
Gene: BSND HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54999182C= , CM000663.2:g.54999182C= GRCh38
NC_000001.10:g.55464855C= , CM000663.1:g.55464855C= GRCh37
NC_000001.9:g.55237443C= NCBI36
NG_008965.1:g.5239C=
NG_008965.2:g.5250C=

Transcript Alleles

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