Canonical Allele Identifier: CA1950145426
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1847838952
gnomAD v4: 11-6390315-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390315G>C , CM000673.2:g.6390315G>C GRCh38
NC_000011.9:g.6411545G>C , CM000673.1:g.6411545G>C GRCh37
NC_000011.8:g.6368121G>C NCBI36
NG_011780.1:g.4891G>C

Transcript Alleles

HGVS Amino-acid Change
XM_005253075.3:c.-284G>C XP_005253132.1:n.-284G>C
XM_011520303.1:c.-284G>C XP_011518605.1:n.-284G>C
XM_011520304.1:c.-284G>C XP_011518606.1:n.-284G>C
XR_930886.1:n.15G>C