Canonical Allele Identifier: CA417956575
Gene: BSND HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.55464940C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54999267C>T , CM000663.2:g.54999267C>T GRCh38
NC_000001.10:g.55464940C>T , CM000663.1:g.55464940C>T GRCh37
NC_000001.9:g.55237528C>T NCBI36
NG_008965.1:g.5324C>T
NG_008965.2:g.5335C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651561.1:c.81C>T MANE Select ENSP00000498282.1:p.Ser27=
ENST00000371265.4:c.81C>T ENSP00000360312.4:p.Ser27=
NM_057176.2:c.81C>T NP_476517.1:p.Ser27=
NM_057176.3:c.81C>T MANE Select NP_476517.1:p.Ser27=
Search 100 bp 5'
Search 100 bp 3'