Canonical Allele Identifier: CA14865685

Gene: S100B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46601141C>T , CM000683.2:g.46601141C>T	GRCh38
NC_000021.8:g.48021054C>T , CM000683.1:g.48021054C>T	GRCh37
NC_000021.7:g.46845482C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291700.9:c.138+1137G>A MANE Select	ENSP00000291700.4:n.138+1137G>A
ENST00000291700.8:c.138+1137G>A	ENSP00000291700.4:n.138+1137G>A
ENST00000367071.4:c.139-766G>A	ENSP00000356038.4:n.139-766G>A
ENST00000397648.1:c.138+1137G>A	ENSP00000380769.1:n.138+1137G>A
NM_006272.2:c.138+1137G>A	NP_006263.1:n.138+1137G>A
XM_017028424.2:c.138+1137G>A	XP_016883913.1:n.138+1137G>A
NM_006272.3:c.138+1137G>A MANE Select	NP_006263.1:n.138+1137G>A