Canonical Allele Identifier: CA2612220860
Gene: SMPD1 HGNC NCBI

Linked Data

gnomAD v4: 11-6390451-T-C

Genomic Alleles

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

Transcript Alleles

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