Canonical Allele Identifier: CA10109561
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs746515729
ExAC: 22:20230074 G / A
gnomAD v2: 22-20230074-G-A
gnomAD v3: 22-20242551-G-A
gnomAD v4: 22-20242551-G-A
COSMIC: COSM4654845
MyVariant Identifiers: chr22:g.20230074G>A (hg19) chr22:g.20242551G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242551G>A , CM000684.2:g.20242551G>A GRCh38
NC_000022.10:g.20230074G>A , CM000684.1:g.20230074G>A GRCh37
NC_000022.9:g.18610074G>A NCBI36
NG_012176.1:g.30743C>T
NG_012176.2:g.30743C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.582C>T MANE Select ENSP00000043402.7:p.Pro194=
ENST00000043402.7:c.582C>T ENSP00000043402.7:p.Pro194=
ENST00000416372.5:c.641C>T
ENST00000425986.1:c.839C>T
NM_023004.5:c.582C>T NP_075380.1:p.Pro194=
NM_023004.6:c.582C>T MANE Select NP_075380.1:p.Pro194=
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