Canonical Allele Identifier: CA410712717
Gene: RTN4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20230148G>C (hg19) chr22:g.20242625G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242625G>C , CM000684.2:g.20242625G>C GRCh38
NC_000022.10:g.20230148G>C , CM000684.1:g.20230148G>C GRCh37
NC_000022.9:g.18610148G>C NCBI36
NG_012176.1:g.30669C>G
NG_012176.2:g.30669C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.508C>G MANE Select ENSP00000043402.7:p.Pro170Ala
ENST00000043402.7:c.508C>G ENSP00000043402.7:p.Pro170Ala
ENST00000416372.5:c.567C>G
ENST00000425986.1:c.765C>G
ENST00000469601.1:n.644C>G
NM_023004.5:c.508C>G NP_075380.1:p.Pro170Ala
NM_023004.6:c.508C>G MANE Select NP_075380.1:p.Pro170Ala
Search 100 bp 5'
Search 100 bp 3'