Canonical Allele Identifier: CA956817
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs377449110
ExAC: 1:94463395 C / T
gnomAD v2: 1-94463395-C-T
gnomAD v3: 1-93997839-C-T
gnomAD v4: 1-93997839-C-T
MyVariant Identifiers: chr1:g.94463395C>T (hg19) chr1:g.93997839C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93997839C>T , CM000663.2:g.93997839C>T GRCh38
NC_000001.10:g.94463395C>T , CM000663.1:g.94463395C>T GRCh37
NC_000001.9:g.94235983C>T NCBI36
NG_009073.1:g.128311G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6729+22G>A MANE Select ENSP00000359245.3:n.6729+22G>A
ENST00000370225.3:c.6729+22G>A ENSP00000359245.3:n.6729+22G>A
ENST00000536513.5:c.3105+22G>A ENSP00000439707.2:n.3105+22G>A
NM_000350.2:c.6729+22G>A NP_000341.2:n.6729+22G>A
NM_000350.3:c.6729+22G>A MANE Select NP_000341.2:n.6729+22G>A
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