Canonical Allele Identifier: CA357603656
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs1405069844
gnomAD v2: 4-88533814-A-G
gnomAD v4: 4-87612662-A-G
MyVariant Identifiers: chr4:g.88533814A>G (hg19) chr4:g.87612662A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612662A>G , CM000666.2:g.87612662A>G GRCh38
NC_000004.11:g.88533814A>G , CM000666.1:g.88533814A>G GRCh37
NC_000004.10:g.88752838A>G NCBI36
NG_011595.1:g.9134A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.476A>G MANE Select ENSP00000498766.1:p.Asp159Gly
ENST00000282478.7:c.476A>G ENSP00000282478.7:p.Asp159Gly
ENST00000399271.5:c.476A>G ENSP00000382213.1:p.Asp159Gly
NM_014208.3:c.476A>G MANE Select NP_055023.2:p.Asp159Gly
Search 100 bp 5'
Search 100 bp 3'