Canonical Allele Identifier: CA2587979487
Gene: RETN HGNC NCBI

Linked Data

gnomAD v4: 19-7669069-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7669069C>A , CM000681.2:g.7669069C>A GRCh38
NC_000019.9:g.7733955C>A , CM000681.1:g.7733955C>A GRCh37
NC_000019.8:g.7639955C>A NCBI36
NG_023447.1:g.4984C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221515.6:c.-63C>A MANE Select ENSP00000221515.1:n.-63C>A
ENST00000221515.5:c.-63C>A ENSP00000221515.1:n.-63C>A
NM_020415.4:c.-63C>A MANE Select NP_065148.1:n.-63C>A
NM_001193374.2:c.-54C>A NP_001180303.1:n.-54C>A
NM_001385725.1:c.-107C>A NP_001372654.1:n.-107C>A
NM_001385726.1:c.-63C>A NP_001372655.1:n.-63C>A
NM_001385727.1:c.-63C>A NP_001372656.1:n.-63C>A
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