Canonical Allele Identifier: CA1474383728
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs1037109925
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87610867C>T , CM000666.2:g.87610867C>T GRCh38
NC_000004.11:g.88532019C>T , CM000666.1:g.88532019C>T GRCh37
NC_000004.10:g.88751043C>T NCBI36
NG_011595.1:g.7339C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.-28-14C>T MANE Select ENSP00000498766.1:n.-28-14C>T
ENST00000399271.5:c.-28-14C>T ENSP00000382213.1:n.-28-14C>T
NM_014208.3:c.-28-14C>T MANE Select NP_055023.2:n.-28-14C>T
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Search 100 bp 3'