Canonical Allele Identifier: CA1950145513
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1590734352

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390451T>G , CM000673.2:g.6390451T>G GRCh38
NC_000011.9:g.6411681T>G , CM000673.1:g.6411681T>G GRCh37
NC_000011.8:g.6368257T>G NCBI36
NG_011780.1:g.5027T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.8:c.-148T>G ENSP00000340409.4:n.-148T>G
ENST00000530395.1:c.-284T>G ENSP00000431479.1:n.-284T>G
ENST00000533196.1:n.12T>G
NM_000543.4:c.-148T>G NP_000534.3:n.-148T>G
NM_001007593.2:c.-148T>G NP_001007594.2:n.-148T>G
XM_005253075.3:c.-148T>G XP_005253132.1:n.-148T>G
XM_011520303.1:c.-148T>G XP_011518605.1:n.-148T>G
XM_011520304.1:c.-148T>G XP_011518606.1:n.-148T>G
XR_930886.1:n.151T>G
NM_001318087.1:c.-148T>G NP_001305016.1:n.-148T>G
NM_001318088.1:c.-1109T>G NP_001305017.1:n.-1109T>G
NR_027400.2:n.38T>G
NR_134502.1:n.38T>G