Canonical Allele Identifier: CA418826620
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94508450G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94042894G>A , CM000663.2:g.94042894G>A GRCh38
NC_000001.10:g.94508450G>A , CM000663.1:g.94508450G>A GRCh37
NC_000001.9:g.94281038G>A NCBI36
NG_009073.1:g.83256C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3195C>T MANE Select ENSP00000359245.3:p.Gly1065=
ENST00000370225.3:c.3195C>T ENSP00000359245.3:p.Gly1065=
ENST00000536513.5:c.-64-2805C>T ENSP00000439707.2:n.-64-2805C>T
NM_000350.2:c.3195C>T NP_000341.2:p.Gly1065=
NM_000350.3:c.3195C>T MANE Select NP_000341.2:p.Gly1065=