Canonical Allele Identifier: CA1950145440
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1847840473
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390333G>A , CM000673.2:g.6390333G>A GRCh38
NC_000011.9:g.6411563G>A , CM000673.1:g.6411563G>A GRCh37
NC_000011.8:g.6368139G>A NCBI36
NG_011780.1:g.4909G>A

Transcript Alleles

HGVS Amino-acid Change
XM_005253075.3:c.-266G>A XP_005253132.1:n.-266G>A
XM_011520303.1:c.-266G>A XP_011518605.1:n.-266G>A
XM_011520304.1:c.-266G>A XP_011518606.1:n.-266G>A
XR_930886.1:n.33G>A
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