Canonical Allele Identifier: CA2321035237
Gene: RETN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7669046C= , CM000681.2:g.7669046C= GRCh38
NC_000019.9:g.7733932C= , CM000681.1:g.7733932C= GRCh37
NC_000019.8:g.7639932C= NCBI36
NG_023447.1:g.4961C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221515.5:c.-86C= ENSP00000221515.1:n.-86C=