Canonical Allele Identifier: CA100849494
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs777011440
MyVariant Identifiers: chr4:g.88533608G>A (hg19) chr4:g.87612456G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612456G>A , CM000666.2:g.87612456G>A GRCh38
NC_000004.11:g.88533608G>A , CM000666.1:g.88533608G>A GRCh37
NC_000004.10:g.88752632G>A NCBI36
NG_011595.1:g.8928G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.270G>A MANE Select ENSP00000498766.1:p.Gly90=
ENST00000282478.7:c.270G>A ENSP00000282478.7:p.Gly90=
ENST00000399271.5:c.270G>A ENSP00000382213.1:p.Gly90=
NM_014208.3:c.270G>A MANE Select NP_055023.2:p.Gly90=
Search 100 bp 5'
Search 100 bp 3'