Canonical Allele Identifier: CA799577336
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs13131929
MyVariant Identifiers: chr4:g.88533441T>A (hg19) chr4:g.87612289T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612289T>A , CM000666.2:g.87612289T>A GRCh38
NC_000004.11:g.88533441T>A , CM000666.1:g.88533441T>A GRCh37
NC_000004.10:g.88752465T>A NCBI36
NG_011595.1:g.8761T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.136-33T>A MANE Select ENSP00000498766.1:n.136-33T>A
ENST00000282478.7:c.136-33T>A ENSP00000282478.7:n.136-33T>A
ENST00000399271.5:c.136-33T>A ENSP00000382213.1:n.136-33T>A
NM_014208.3:c.136-33T>A MANE Select NP_055023.2:n.136-33T>A
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