Canonical Allele Identifier: CA2587979499
Gene: RETN HGNC NCBI

Linked Data

gnomAD v4: 19-7669074-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7669074G>T , CM000681.2:g.7669074G>T GRCh38
NC_000019.9:g.7733960G>T , CM000681.1:g.7733960G>T GRCh37
NC_000019.8:g.7639960G>T NCBI36
NG_023447.1:g.4989G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221515.6:c.-58G>T MANE Select ENSP00000221515.1:n.-58G>T
ENST00000221515.5:c.-58G>T ENSP00000221515.1:n.-58G>T
NM_020415.4:c.-58G>T MANE Select NP_065148.1:n.-58G>T
NM_001193374.2:c.-49G>T NP_001180303.1:n.-49G>T
NM_001385725.1:c.-102G>T NP_001372654.1:n.-102G>T
NM_001385726.1:c.-58G>T NP_001372655.1:n.-58G>T
NM_001385727.1:c.-58G>T NP_001372656.1:n.-58G>T
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