Canonical Allele Identifier: CA393032658
Gene: NR2E3 HGNC NCBI

Linked Data

gnomAD v4: 15-71811827-T-C
MyVariant Identifiers: chr15:g.72104167T>C (hg19) chr15:g.71811827T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811827T>C , CM000677.2:g.71811827T>C GRCh38
NC_000015.9:g.72104167T>C , CM000677.1:g.72104167T>C GRCh37
NC_000015.8:g.69891221T>C NCBI36
NG_009113.2:g.6273T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.307T>C MANE Select ENSP00000482504.1:p.Cys103Arg
ENST00000617575.4:c.307T>C ENSP00000482504.1:p.Cys103Arg
ENST00000621098.1:c.307T>C ENSP00000479962.1:p.Cys103Arg
ENST00000621736.4:c.43T>C ENSP00000479254.1:p.Cys15Arg
NM_014249.3:c.307T>C NP_055064.1:p.Cys103Arg
NM_016346.3:c.307T>C NP_057430.1:p.Cys103Arg
XM_011521146.1:c.43T>C XP_011519448.1:p.Cys15Arg
NM_014249.4:c.307T>C MANE Select NP_055064.1:p.Cys103Arg
NM_016346.4:c.307T>C NP_057430.1:p.Cys103Arg
Search 100 bp 5'
Search 100 bp 3'