Canonical Allele Identifier: CA799576992
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs1479315777
gnomAD v4: 4-87612011-T-G
MyVariant Identifiers: chr4:g.88533163T>G (hg19) chr4:g.87612011T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612011T>G , CM000666.2:g.87612011T>G GRCh38
NC_000004.11:g.88533163T>G , CM000666.1:g.88533163T>G GRCh37
NC_000004.10:g.88752187T>G NCBI36
NG_011595.1:g.8483T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.52-94T>G MANE Select ENSP00000498766.1:n.52-94T>G
ENST00000282478.7:c.52-94T>G ENSP00000282478.7:n.52-94T>G
ENST00000399271.5:c.52-94T>G ENSP00000382213.1:n.52-94T>G
NM_014208.3:c.52-94T>G MANE Select NP_055023.2:n.52-94T>G
Search 100 bp 5'
Search 100 bp 3'