Canonical Allele Identifier: CA2671358095
Gene: DSPP HGNC NCBI

Linked Data

gnomAD v4: 4-87610859-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87610859G>C , CM000666.2:g.87610859G>C GRCh38
NC_000004.11:g.88532011G>C , CM000666.1:g.88532011G>C GRCh37
NC_000004.10:g.88751035G>C NCBI36
NG_011595.1:g.7331G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.-28-22G>C MANE Select ENSP00000498766.1:n.-28-22G>C
ENST00000399271.5:c.-28-22G>C ENSP00000382213.1:n.-28-22G>C
NM_014208.3:c.-28-22G>C MANE Select NP_055023.2:n.-28-22G>C
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