Canonical Allele Identifier: CA2392757374
Gene: S100B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46599906_46599907delinsAT , CM000683.2:g.46599906_46599907delinsAT GRCh38
NC_000021.8:g.48019819_48019820delinsAT , CM000683.1:g.48019819_48019820delinsAT GRCh37
NC_000021.7:g.46844247_46844248delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000291700.9:c.139-404_139-403delinsAT MANE Select ENSP00000291700.4:n.139-404_139-403delinsAT
ENST00000291700.8:c.139-404_139-403delinsAT ENSP00000291700.4:n.139-404_139-403delinsAT
ENST00000367071.4:c.232+375_232+376delinsAT ENSP00000356038.4:n.232+375_232+376delinsAT
ENST00000397648.1:c.139-404_139-403delinsAT ENSP00000380769.1:n.139-404_139-403delinsAT
NM_006272.2:c.139-404_139-403delinsAT NP_006263.1:n.139-404_139-403delinsAT
XM_017028424.2:c.139-404_139-403delinsAT XP_016883913.1:n.139-404_139-403delinsAT
NM_006272.3:c.139-404_139-403delinsAT MANE Select NP_006263.1:n.139-404_139-403delinsAT
Search 100 bp 5'
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