Canonical Allele Identifier: CA2587979444
Gene: RETN HGNC NCBI

Linked Data

gnomAD v4: 19-7669045-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7669045C>A , CM000681.2:g.7669045C>A GRCh38
NC_000019.9:g.7733931C>A , CM000681.1:g.7733931C>A GRCh37
NC_000019.8:g.7639931C>A NCBI36
NG_023447.1:g.4960C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221515.5:c.-87C>A ENSP00000221515.1:n.-87C>A
Search 100 bp 5'
Search 100 bp 3'