Canonical Allele Identifier: CA3000831
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs781728187
ExAC: 4:88533440 A / C
gnomAD v2: 4-88533440-A-C
MyVariant Identifiers: chr4:g.88533440A>C (hg19) chr4:g.87612288A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612288A>C , CM000666.2:g.87612288A>C GRCh38
NC_000004.11:g.88533440A>C , CM000666.1:g.88533440A>C GRCh37
NC_000004.10:g.88752464A>C NCBI36
NG_011595.1:g.8760A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.136-34A>C MANE Select ENSP00000498766.1:n.136-34A>C
ENST00000282478.7:c.136-34A>C ENSP00000282478.7:n.136-34A>C
ENST00000399271.5:c.136-34A>C ENSP00000382213.1:n.136-34A>C
NM_014208.3:c.136-34A>C MANE Select NP_055023.2:n.136-34A>C
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