Canonical Allele Identifier: CA340470708
Gene: BSND HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.55464960A>C (hg19) chr1:g.54999287A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54999287A>C , CM000663.2:g.54999287A>C GRCh38
NC_000001.10:g.55464960A>C , CM000663.1:g.55464960A>C GRCh37
NC_000001.9:g.55237548A>C NCBI36
NG_008965.1:g.5344A>C
NG_008965.2:g.5355A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651561.1:c.101A>C MANE Select ENSP00000498282.1:p.Tyr34Ser
ENST00000371265.4:c.101A>C ENSP00000360312.4:p.Tyr34Ser
NM_057176.2:c.101A>C NP_476517.1:p.Tyr34Ser
NM_057176.3:c.101A>C MANE Select NP_476517.1:p.Tyr34Ser
Search 100 bp 5'
Search 100 bp 3'