Canonical Allele Identifier: CA2587979484
Gene: RETN HGNC NCBI

Linked Data

gnomAD v4: 19-7669067-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7669067A>G , CM000681.2:g.7669067A>G GRCh38
NC_000019.9:g.7733953A>G , CM000681.1:g.7733953A>G GRCh37
NC_000019.8:g.7639953A>G NCBI36
NG_023447.1:g.4982A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221515.6:c.-65A>G MANE Select ENSP00000221515.1:n.-65A>G
ENST00000221515.5:c.-65A>G ENSP00000221515.1:n.-65A>G
NM_020415.4:c.-65A>G MANE Select NP_065148.1:n.-65A>G
NM_001193374.2:c.-56A>G NP_001180303.1:n.-56A>G
NM_001385725.1:c.-109A>G NP_001372654.1:n.-109A>G
NM_001385726.1:c.-65A>G NP_001372655.1:n.-65A>G
NM_001385727.1:c.-65A>G NP_001372656.1:n.-65A>G
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