Canonical Allele Identifier: CA1950145437
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1159213466
gnomAD v4: 11-6390328-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390328G>A , CM000673.2:g.6390328G>A GRCh38
NC_000011.9:g.6411558G>A , CM000673.1:g.6411558G>A GRCh37
NC_000011.8:g.6368134G>A NCBI36
NG_011780.1:g.4904G>A

Transcript Alleles

HGVS Amino-acid Change
XM_005253075.3:c.-271G>A XP_005253132.1:n.-271G>A
XM_011520303.1:c.-271G>A XP_011518605.1:n.-271G>A
XM_011520304.1:c.-271G>A XP_011518606.1:n.-271G>A
XR_930886.1:n.28G>A
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