Canonical Allele Identifier: CA393032064
Gene: NR2E3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.72103886T>C (hg19) chr15:g.71811546T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811546T>C , CM000677.2:g.71811546T>C GRCh38
NC_000015.9:g.72103886T>C , CM000677.1:g.72103886T>C GRCh37
NC_000015.8:g.69890940T>C NCBI36
NG_009113.2:g.5992T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.182T>C MANE Select ENSP00000482504.1:p.Ile61Thr
ENST00000617575.4:c.182T>C ENSP00000482504.1:p.Ile61Thr
ENST00000621098.1:c.182T>C ENSP00000479962.1:p.Ile61Thr
ENST00000621736.4:c.-83T>C ENSP00000479254.1:n.-83T>C
NM_014249.3:c.182T>C NP_055064.1:p.Ile61Thr
NM_016346.3:c.182T>C NP_057430.1:p.Ile61Thr
XM_011521146.1:c.-83T>C XP_011519448.1:n.-83T>C
NM_014249.4:c.182T>C MANE Select NP_055064.1:p.Ile61Thr
NM_016346.4:c.182T>C NP_057430.1:p.Ile61Thr
Search 100 bp 5'
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