Canonical Allele Identifier: CA1950145494
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390418G= , CM000673.2:g.6390418G= GRCh38
NC_000011.9:g.6411648G= , CM000673.1:g.6411648G= GRCh37
NC_000011.8:g.6368224G= NCBI36
NG_011780.1:g.4994G=

Transcript Alleles

HGVS Amino-acid Change
NM_000543.4:c.-181G= NP_000534.3:n.-181G=
NM_001007593.2:c.-181G= NP_001007594.2:n.-181G=
XM_005253075.3:c.-181G= XP_005253132.1:n.-181G=
XM_011520303.1:c.-181G= XP_011518605.1:n.-181G=
XM_011520304.1:c.-181G= XP_011518606.1:n.-181G=
XR_930886.1:n.118G=
NM_001318087.1:c.-181G= NP_001305016.1:n.-181G=
NM_001318088.1:c.-1142G= NP_001305017.1:n.-1142G=
NR_027400.2:n.5G=
NR_134502.1:n.5G=