Canonical Allele Identifier: CA10109608
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs775520463
ExAC: 22:20230310 C / A
gnomAD v2: 22-20230310-C-A
gnomAD v4: 22-20242787-C-A
MyVariant Identifiers: chr22:g.20230310C>A (hg19) chr22:g.20242787C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242787C>A , CM000684.2:g.20242787C>A GRCh38
NC_000022.10:g.20230310C>A , CM000684.1:g.20230310C>A GRCh37
NC_000022.9:g.18610310C>A NCBI36
NG_012176.1:g.30507G>T
NG_012176.2:g.30507G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.346G>T MANE Select ENSP00000043402.7:p.Ala116Ser
ENST00000043402.7:c.346G>T ENSP00000043402.7:p.Ala116Ser
ENST00000416372.5:c.405G>T
ENST00000425986.1:c.603G>T
ENST00000469601.1:n.482G>T
NM_023004.5:c.346G>T NP_075380.1:p.Ala116Ser
NM_023004.6:c.346G>T MANE Select NP_075380.1:p.Ala116Ser
Search 100 bp 5'
Search 100 bp 3'