Canonical Allele Identifier: CA2321035243
Gene: RETN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7669055C= , CM000681.2:g.7669055C= GRCh38
NC_000019.9:g.7733941C= , CM000681.1:g.7733941C= GRCh37
NC_000019.8:g.7639941C= NCBI36
NG_023447.1:g.4970C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221515.6:c.-77C= MANE Select ENSP00000221515.1:n.-77C=
ENST00000221515.5:c.-77C= ENSP00000221515.1:n.-77C=
NM_020415.4:c.-77C= MANE Select NP_065148.1:n.-77C=
NM_001193374.2:c.-68C= NP_001180303.1:n.-68C=
NM_001385725.1:c.-121C= NP_001372654.1:n.-121C=
NM_001385726.1:c.-77C= NP_001372655.1:n.-77C=
NM_001385727.1:c.-77C= NP_001372656.1:n.-77C=
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