Canonical Allele Identifier: CA10109540
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs754793885
ExAC: 22:20229977 G / T
gnomAD v2: 22-20229977-G-T
gnomAD v4: 22-20242454-G-T
MyVariant Identifiers: chr22:g.20229977G>T (hg19) chr22:g.20242454G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242454G>T , CM000684.2:g.20242454G>T GRCh38
NC_000022.10:g.20229977G>T , CM000684.1:g.20229977G>T GRCh37
NC_000022.9:g.18609977G>T NCBI36
NG_012176.1:g.30840C>A
NG_012176.2:g.30840C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.679C>A MANE Select ENSP00000043402.7:p.Arg227Ser
ENST00000043402.7:c.679C>A ENSP00000043402.7:p.Arg227Ser
ENST00000416372.5:c.738C>A
ENST00000425986.1:c.936C>A
NM_023004.5:c.679C>A NP_075380.1:p.Arg227Ser
NM_023004.6:c.679C>A MANE Select NP_075380.1:p.Arg227Ser
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