Canonical Allele Identifier: CA227441
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 99489
ClinVar RCV Id: RCV000085850 RCV000248334
dbSNP Id: rs1800699
ExAC: 1:94463396 G / A
gnomAD v2: 1-94463396-G-A
gnomAD v3: 1-93997840-G-A
gnomAD v4: 1-93997840-G-A
MyVariant Identifiers: chr1:g.94463396G>A (hg19) chr1:g.93997840G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93997840G>A , CM000663.2:g.93997840G>A GRCh38
NC_000001.10:g.94463396G>A , CM000663.1:g.94463396G>A GRCh37
NC_000001.9:g.94235984G>A NCBI36
NG_009073.1:g.128310C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6729+21C>T MANE Select ENSP00000359245.3:n.6729+21C>T
ENST00000370225.3:c.6729+21C>T ENSP00000359245.3:n.6729+21C>T
ENST00000536513.5:c.3105+21C>T ENSP00000439707.2:n.3105+21C>T
NM_000350.2:c.6729+21C>T NP_000341.2:n.6729+21C>T
NM_000350.3:c.6729+21C>T MANE Select NP_000341.2:n.6729+21C>T
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