Canonical Allele Identifier: CA357603489
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs1727757942
gnomAD v4: 4-87612589-G-A
MyVariant Identifiers: chr4:g.88533741G>A (hg19) chr4:g.87612589G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612589G>A , CM000666.2:g.87612589G>A GRCh38
NC_000004.11:g.88533741G>A , CM000666.1:g.88533741G>A GRCh37
NC_000004.10:g.88752765G>A NCBI36
NG_011595.1:g.9061G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.403G>A MANE Select ENSP00000498766.1:p.Gly135Ser
ENST00000282478.7:c.403G>A ENSP00000282478.7:p.Gly135Ser
ENST00000399271.5:c.403G>A ENSP00000382213.1:p.Gly135Ser
NM_014208.3:c.403G>A MANE Select NP_055023.2:p.Gly135Ser
Search 100 bp 5'
Search 100 bp 3'