Canonical Allele Identifier: CA440294080
Gene: DSPP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88533521G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612369G>C , CM000666.2:g.87612369G>C GRCh38
NC_000004.11:g.88533521G>C , CM000666.1:g.88533521G>C GRCh37
NC_000004.10:g.88752545G>C NCBI36
NG_011595.1:g.8841G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.183G>C MANE Select ENSP00000498766.1:p.Val61=
ENST00000282478.7:c.183G>C ENSP00000282478.7:p.Val61=
ENST00000399271.5:c.183G>C ENSP00000382213.1:p.Val61=
NM_014208.3:c.183G>C MANE Select NP_055023.2:p.Val61=
Search 100 bp 5'
Search 100 bp 3'