Canonical Allele Identifier: CA217298813
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs966023249
gnomAD v4: 11-6390378-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390378T>C , CM000673.2:g.6390378T>C GRCh38
NC_000011.9:g.6411608T>C , CM000673.1:g.6411608T>C GRCh37
NC_000011.8:g.6368184T>C NCBI36
NG_011780.1:g.4954T>C

Transcript Alleles

HGVS Amino-acid Change
XM_005253075.3:c.-221T>C XP_005253132.1:n.-221T>C
XM_011520303.1:c.-221T>C XP_011518605.1:n.-221T>C
XM_011520304.1:c.-221T>C XP_011518606.1:n.-221T>C
XR_930886.1:n.78T>C