Canonical Allele Identifier: CA26851991

Gene: ABCA4

Linked Data

• dbSNP Id: rs774052760
• gnomAD v2: 1-94533251-C-G
• gnomAD v3: 1-94067695-C-G
• gnomAD v4: 1-94067695-C-G
• MyVariant Identifiers: chr1:g.94533251C>G (hg19) ; chr1:g.94067695C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94067695C>G , CM000663.2:g.94067695C>G	GRCh38
NC_000001.10:g.94533251C>G , CM000663.1:g.94533251C>G	GRCh37
NC_000001.9:g.94305839C>G	NCBI36
NG_009073.1:g.58455G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.1555-4378G>C MANE Select	ENSP00000359245.3:n.1555-4378G>C
ENST00000649773.1:c.1555-4378G>C	ENSP00000496882.1:n.1555-4378G>C
ENST00000370225.3:c.1555-4378G>C	ENSP00000359245.3:n.1555-4378G>C
NM_000350.2:c.1555-4378G>C	NP_000341.2:n.1555-4378G>C
NM_000350.3:c.1555-4378G>C MANE Select	NP_000341.2:n.1555-4378G>C