Canonical Allele Identifier: CA740500774

Gene: ABCA4

Linked Data

• dbSNP Id: rs1291930022
• MyVariant Identifiers: chr1:g.94463403C>A (hg19) ; chr1:g.93997847C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.93997847C>A , CM000663.2:g.93997847C>A	GRCh38
NC_000001.10:g.94463403C>A , CM000663.1:g.94463403C>A	GRCh37
NC_000001.9:g.94235991C>A	NCBI36
NG_009073.1:g.128303G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370225.4:c.6729+14G>T MANE Select	ENSP00000359245.3:n.6729+14G>T
ENST00000370225.3:c.6729+14G>T	ENSP00000359245.3:n.6729+14G>T
ENST00000536513.5:c.3105+14G>T	ENSP00000439707.2:n.3105+14G>T
NM_000350.2:c.6729+14G>T	NP_000341.2:n.6729+14G>T
NM_000350.3:c.6729+14G>T MANE Select	NP_000341.2:n.6729+14G>T