Canonical Allele Identifier: CA10648834

Gene: RTN2

Linked Data

• ClinVar Variation Id: 329545
• ClinVar RCV Id: RCV000263193
• dbSNP Id: rs886054503
• gnomAD v4: 19-45485560-C-T
• MyVariant Identifiers: chr19:g.45988818C>T (hg19) ; chr19:g.45485560C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45485560C>T , CM000681.2:g.45485560C>T	GRCh38
NC_000019.9:g.45988818C>T , CM000681.1:g.45988818C>T	GRCh37
NC_000019.8:g.50680658C>T	NCBI36
NG_032157.1:g.16494G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245923.9:c.*148G>A MANE Select	ENSP00000245923.3:n.*148G>A
ENST00000245923.8:c.*148G>A	ENSP00000245923.3:n.*148G>A
ENST00000344680.8:c.*148G>A	ENSP00000345127.3:n.*148G>A
ENST00000430715.6:c.*148G>A	ENSP00000398178.1:n.*148G>A
ENST00000587597.5:c.*330G>A	ENSP00000468144.1:n.*330G>A
ENST00000590526.5:c.*148G>A	ENSP00000466619.1:n.*148G>A
ENST00000591286.5:c.*784G>A	ENSP00000467863.1:n.*784G>A
NM_005619.4:c.*148G>A	NP_005610.1:n.*148G>A
NM_206900.2:c.*148G>A	NP_996783.1:n.*148G>A
NM_206901.2:c.*148G>A	NP_996784.1:n.*148G>A
NM_005619.5:c.*148G>A MANE Select	NP_005610.1:n.*148G>A
NM_206900.3:c.*148G>A	NP_996783.1:n.*148G>A
NM_206901.3:c.*148G>A	NP_996784.1:n.*148G>A