Canonical Allele Identifier: CA341276270
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-93997886-G-C
MyVariant Identifiers: chr1:g.94463442G>C (hg19) chr1:g.93997886G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93997886G>C , CM000663.2:g.93997886G>C GRCh38
NC_000001.10:g.94463442G>C , CM000663.1:g.94463442G>C GRCh37
NC_000001.9:g.94236030G>C NCBI36
NG_009073.1:g.128264C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6704C>G MANE Select ENSP00000359245.3:p.Ser2235Ter
ENST00000370225.3:c.6704C>G ENSP00000359245.3:p.Ser2235Ter
ENST00000536513.5:c.3080C>G ENSP00000439707.2:p.Ser1027Ter
NM_000350.2:c.6704C>G NP_000341.2:p.Ser2235Ter
NM_000350.3:c.6704C>G MANE Select NP_000341.2:p.Ser2235Ter
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