Canonical Allele Identifier: CA2580671007
Gene: S100B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46599955G>T , CM000683.2:g.46599955G>T GRCh38
NC_000021.8:g.48019868G>T , CM000683.1:g.48019868G>T GRCh37
NC_000021.7:g.46844296G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000291700.9:c.139-452C>A MANE Select ENSP00000291700.4:n.139-452C>A
ENST00000291700.8:c.139-452C>A ENSP00000291700.4:n.139-452C>A
ENST00000367071.4:c.232+327C>A ENSP00000356038.4:n.232+327C>A
ENST00000397648.1:c.139-452C>A ENSP00000380769.1:n.139-452C>A
NM_006272.2:c.139-452C>A NP_006263.1:n.139-452C>A
XM_017028424.2:c.139-452C>A XP_016883913.1:n.139-452C>A
NM_006272.3:c.139-452C>A MANE Select NP_006263.1:n.139-452C>A
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