Canonical Allele Identifier: CA418825783
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94577011T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94111455T>G , CM000663.2:g.94111455T>G GRCh38
NC_000001.10:g.94577011T>G , CM000663.1:g.94577011T>G GRCh37
NC_000001.9:g.94349599T>G NCBI36
NG_009073.1:g.14695A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.285A>C MANE Select ENSP00000359245.3:p.Ser95=
ENST00000649773.1:c.285A>C ENSP00000496882.1:p.Ser95=
ENST00000370225.3:c.285A>C ENSP00000359245.3:p.Ser95=
NM_000350.2:c.285A>C NP_000341.2:p.Ser95=
NM_000350.3:c.285A>C MANE Select NP_000341.2:p.Ser95=