Canonical Allele Identifier: CA858083880
Gene: ABCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1396686657
MyVariant Identifiers: chr9:g.107690454T>C (hg19) chr9:g.104928173T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928173T>C , CM000671.2:g.104928173T>C GRCh38
NC_000009.11:g.107690454T>C , CM000671.1:g.107690454T>C GRCh37
NC_000009.10:g.106730275T>C NCBI36
NG_007981.1:g.4983A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374736.7:c.-331A>G ENSP00000363868.3:n.-331A>G
NM_005502.3:c.-331A>G NP_005493.2:n.-331A>G
XM_011518342.1:c.-394A>G XP_011516644.1:n.-394A>G
XR_930204.1:n.734+263T>C
XM_011518342.3:c.-394A>G XP_011516644.1:n.-394A>G
XR_930204.2:n.115+263T>C
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