Canonical Allele Identifier: CA1950145466
Gene: SMPD1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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