Canonical Allele Identifier: CA10628717
Gene: ABCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 364482
dbSNP Id: rs886063317

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928185T>G , CM000671.2:g.104928185T>G GRCh38
NC_000009.11:g.107690466T>G , CM000671.1:g.107690466T>G GRCh37
NC_000009.10:g.106730287T>G NCBI36
NG_007981.1:g.4971A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374736.7:c.-343A>C ENSP00000363868.3:n.-343A>C
NM_005502.3:c.-343A>C NP_005493.2:n.-343A>C
XM_011518342.1:c.-406A>C XP_011516644.1:n.-406A>C
XR_930204.1:n.734+275T>G
XM_011518342.3:c.-406A>C XP_011516644.1:n.-406A>C
XR_930204.2:n.115+275T>G