Canonical Allele Identifier: CA1022924658
Gene: S100B HGNC NCBI

Linked Data

dbSNP Id: rs2061036917
gnomAD v3: 21-46599932-T-C
gnomAD v4: 21-46599932-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46599932T>C , CM000683.2:g.46599932T>C GRCh38
NC_000021.8:g.48019845T>C , CM000683.1:g.48019845T>C GRCh37
NC_000021.7:g.46844273T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000291700.9:c.139-429A>G MANE Select ENSP00000291700.4:n.139-429A>G
ENST00000291700.8:c.139-429A>G ENSP00000291700.4:n.139-429A>G
ENST00000367071.4:c.232+350A>G ENSP00000356038.4:n.232+350A>G
ENST00000397648.1:c.139-429A>G ENSP00000380769.1:n.139-429A>G
NM_006272.2:c.139-429A>G NP_006263.1:n.139-429A>G
XM_017028424.2:c.139-429A>G XP_016883913.1:n.139-429A>G
NM_006272.3:c.139-429A>G MANE Select NP_006263.1:n.139-429A>G
Search 100 bp 5'
Search 100 bp 3'