Canonical Allele Identifier: CA1950145422
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1847838796
gnomAD v4: 11-6390313-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390313C>T , CM000673.2:g.6390313C>T GRCh38
NC_000011.9:g.6411543C>T , CM000673.1:g.6411543C>T GRCh37
NC_000011.8:g.6368119C>T NCBI36
NG_011780.1:g.4889C>T

Transcript Alleles

HGVS Amino-acid Change
XM_005253075.3:c.-286C>T XP_005253132.1:n.-286C>T
XM_011520303.1:c.-286C>T XP_011518605.1:n.-286C>T
XM_011520304.1:c.-286C>T XP_011518606.1:n.-286C>T
XR_930886.1:n.13C>T