Canonical Allele Identifier: CA410712875

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230193C>A (hg19) ; chr22:g.20242670C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242670C>A , CM000684.2:g.20242670C>A	GRCh38
NC_000022.10:g.20230193C>A , CM000684.1:g.20230193C>A	GRCh37
NC_000022.9:g.18610193C>A	NCBI36
NG_012176.1:g.30624G>T
NG_012176.2:g.30624G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.463G>T MANE Select	ENSP00000043402.7:p.Ala155Ser
ENST00000043402.7:c.463G>T	ENSP00000043402.7:p.Ala155Ser
ENST00000416372.5:c.522G>T
ENST00000425986.1:c.720G>T
ENST00000469601.1:n.599G>T
NM_023004.5:c.463G>T	NP_075380.1:p.Ala155Ser
NM_023004.6:c.463G>T MANE Select	NP_075380.1:p.Ala155Ser