Canonical Allele Identifier: CA513693150
Gene: RTN4R HGNC NCBI

Linked Data

gnomAD v4: 22-20242779-G-C
MyVariant Identifiers: chr22:g.20230302G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242779G>C , CM000684.2:g.20242779G>C GRCh38
NC_000022.10:g.20230302G>C , CM000684.1:g.20230302G>C GRCh37
NC_000022.9:g.18610302G>C NCBI36
NG_012176.1:g.30515C>G
NG_012176.2:g.30515C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.354C>G MANE Select ENSP00000043402.7:p.Leu118=
ENST00000043402.7:c.354C>G ENSP00000043402.7:p.Leu118=
ENST00000416372.5:c.413C>G
ENST00000425986.1:c.611C>G
ENST00000469601.1:n.490C>G
NM_023004.5:c.354C>G NP_075380.1:p.Leu118=
NM_023004.6:c.354C>G MANE Select NP_075380.1:p.Leu118=
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Search 100 bp 3'