Canonical Allele Identifier: CA12700816
Gene: CD36 HGNC NCBI

Linked Data

dbSNP Id: rs10499859
gnomAD v2: 7-80258810-A-G
gnomAD v3: 7-80629494-A-G
gnomAD v4: 7-80629494-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.80629494A>G , CM000669.2:g.80629494A>G GRCh38
NC_000007.13:g.80258810A>G , CM000669.1:g.80258810A>G GRCh37
NC_000007.12:g.80096746A>G NCBI36
NG_008192.1:g.32307A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000309881.11:c.-183-16594A>G ENSP00000308165.7:n.-183-16594A>G
ENST00000428497.5:c.-184+3262A>G ENSP00000409762.1:n.-184+3262A>G
ENST00000435819.5:c.-183-16594A>G ENSP00000399421.1:n.-183-16594A>G
ENST00000436384.5:c.-184+4454A>G ENSP00000398760.1:n.-184+4454A>G
ENST00000438020.5:c.-184+5304A>G ENSP00000410371.1:n.-184+5304A>G
ENST00000478292.2:n.297-3703A>G
ENST00000480599.6:n.231-16594A>G
ENST00000526804.5:n.156-7338A>G
ENST00000534394.5:c.-108-27046A>G ENSP00000431296.1:n.-108-27046A>G
NM_001001547.2:c.-183-16594A>G NP_001001547.1:n.-183-16594A>G
NM_001289911.1:c.-108-27046A>G NP_001276840.1:n.-108-27046A>G
XM_005250713.1:c.-183-16594A>G XP_005250770.1:n.-183-16594A>G
XM_005250714.1:c.-184+5304A>G XP_005250771.1:n.-184+5304A>G
XM_024447003.1:c.-183-16594A>G XP_024302771.1:n.-183-16594A>G
NM_001001547.3:c.-183-16594A>G NP_001001547.1:n.-183-16594A>G
NM_001289911.2:c.-108-27046A>G NP_001276840.1:n.-108-27046A>G
NM_001371074.1:c.-179-16598A>G NP_001358003.1:n.-179-16598A>G
NM_001371075.1:c.-183-16594A>G NP_001358004.1:n.-183-16594A>G
NM_001371077.1:c.-184+5304A>G NP_001358006.1:n.-184+5304A>G
NM_001371078.1:c.-184+5304A>G NP_001358007.1:n.-184+5304A>G
NM_001371080.1:c.-185+27115A>G NP_001358009.1:n.-185+27115A>G
NM_001371081.1:c.-665-16594A>G NP_001358010.1:n.-665-16594A>G