Canonical Allele Identifier: CA341276149
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2733935
ClinVar RCV Id: RCV003562265
MyVariant Identifiers: chr1:g.94517226G>C (hg19) chr1:g.94051670G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94051670G>C , CM000663.2:g.94051670G>C GRCh38
NC_000001.10:g.94517226G>C , CM000663.1:g.94517226G>C GRCh37
NC_000001.9:g.94289814G>C NCBI36
NG_009073.1:g.74480C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2616C>G MANE Select ENSP00000359245.3:p.Tyr872Ter
ENST00000649773.1:c.2394C>G ENSP00000496882.1:p.Tyr798Ter
ENST00000370225.3:c.2616C>G ENSP00000359245.3:p.Tyr872Ter
ENST00000536513.5:c.-65+11504C>G ENSP00000439707.2:n.-65+11504C>G
NM_000350.2:c.2616C>G NP_000341.2:p.Tyr872Ter
NM_000350.3:c.2616C>G MANE Select NP_000341.2:p.Tyr872Ter
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