Canonical Allele Identifier: CA14646802
Gene: CD33 HGNC NCBI
dbSNP:
3865444
gnomAD v2:
19:51727962 C / A
gnomAD v3:
19:51224706 C / A
gnomAD v4:
chr19-51224706-C-A
Joint Max Group AF 0.41910214 (AMR)
Genomes Max Group AF 0.41910214 (AMR)
MyVariant.info:
GRCh38 chr19:g.51224706C>A
GRCh37 chr19:g.51727962C>A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51224706C>A , CM000681.2:g.51224706C>A GRCh38
NC_000019.9:g.51727962C>A , CM000681.1:g.51727962C>A GRCh37
NC_000019.8:g.56419774C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011527531.1:c.-1C>A XP_011525833.1:n.-1C>A
XM_011527532.1:c.-38C>A XP_011525834.1:n.-38C>A
XR_935875.1:n.72C>A
XM_011527531.2:c.-1C>A XP_011525833.1:n.-1C>A
XM_011527532.2:c.-38C>A XP_011525834.1:n.-38C>A
XM_017027508.1:c.-1C>A XP_016882997.1:n.-1C>A
XM_017027509.1:c.-1C>A XP_016882998.1:n.-1C>A
XM_017027510.1:c.-1C>A XP_016882999.1:n.-1C>A
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