Canonical Allele Identifier: CA341279274
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1661159791

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062605T>C , CM000663.2:g.94062605T>C GRCh38
NC_000001.10:g.94528161T>C , CM000663.1:g.94528161T>C GRCh37
NC_000001.9:g.94300749T>C NCBI36
NG_009073.1:g.63545A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1909A>G MANE Select ENSP00000359245.3:p.Met637Val
ENST00000649773.1:c.1909A>G ENSP00000496882.1:p.Met637Val
ENST00000370225.3:c.1909A>G ENSP00000359245.3:p.Met637Val
ENST00000536513.5:c.-65+569A>G ENSP00000439707.2:n.-65+569A>G
NM_000350.2:c.1909A>G NP_000341.2:p.Met637Val
NM_000350.3:c.1909A>G MANE Select NP_000341.2:p.Met637Val