Canonical Allele Identifier: CA871183
Gene: BSND HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54999153G>A , CM000663.2:g.54999153G>A GRCh38
NC_000001.10:g.55464826G>A , CM000663.1:g.55464826G>A GRCh37
NC_000001.9:g.55237414G>A NCBI36
NG_008965.1:g.5210G>A
NG_008965.2:g.5221G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651561.1:c.-34G>A MANE Select ENSP00000498282.1:n.-34G>A
ENST00000371265.4:c.-34G>A ENSP00000360312.4:n.-34G>A
NM_057176.2:c.-34G>A NP_476517.1:n.-34G>A
NM_057176.3:c.-34G>A MANE Select NP_476517.1:n.-34G>A