Canonical Allele Identifier: CA15311993
Gene: S100P HGNC NCBI

Linked Data

dbSNP Id: rs3822262
gnomAD v2: 4-6697766-T-G
gnomAD v3: 4-6696039-T-G
gnomAD v4: 4-6696039-T-G
MyVariant Identifiers: chr4:g.6697766T>G (hg19) chr4:g.6696039T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6696039T>G , CM000666.2:g.6696039T>G GRCh38
NC_000004.11:g.6697766T>G , CM000666.1:g.6697766T>G GRCh37
NC_000004.10:g.6748667T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296370.4:c.139-854T>G MANE Select ENSP00000296370.3:n.139-854T>G
ENST00000296370.3:c.139-854T>G ENSP00000296370.3:n.139-854T>G
ENST00000513778.1:n.36-854T>G
NM_005980.2:c.139-854T>G NP_005971.1:n.139-854T>G
NM_005980.3:c.139-854T>G MANE Select NP_005971.1:n.139-854T>G
Search 100 bp 5'
Search 100 bp 3'