Canonical Allele Identifier: CA340470458
Gene: BSND HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54999199A>G , CM000663.2:g.54999199A>G GRCh38
NC_000001.10:g.55464872A>G , CM000663.1:g.55464872A>G GRCh37
NC_000001.9:g.55237460A>G NCBI36
NG_008965.1:g.5256A>G
NG_008965.2:g.5267A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651561.1:c.13A>G MANE Select ENSP00000498282.1:p.Lys5Glu
ENST00000371265.4:c.13A>G ENSP00000360312.4:p.Lys5Glu
NM_057176.2:c.13A>G NP_476517.1:p.Lys5Glu
NM_057176.3:c.13A>G MANE Select NP_476517.1:p.Lys5Glu