Canonical Allele Identifier: CA217298809
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs762079020
MyVariant Identifiers: chr11:g.6411587G>C (hg19) chr11:g.6390357G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390357G>C , CM000673.2:g.6390357G>C GRCh38
NC_000011.9:g.6411587G>C , CM000673.1:g.6411587G>C GRCh37
NC_000011.8:g.6368163G>C NCBI36
NG_011780.1:g.4933G>C

Transcript Alleles

HGVS Amino-acid Change
XM_005253075.3:c.-242G>C XP_005253132.1:n.-242G>C
XM_011520303.1:c.-242G>C XP_011518605.1:n.-242G>C
XM_011520304.1:c.-242G>C XP_011518606.1:n.-242G>C
XR_930886.1:n.57G>C
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