Canonical Allele Identifier: CA2735817766
Gene: RLN3 HGNC NCBI

Linked Data

dbSNP Id: rs2145680589
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.14029014A>G , CM000681.2:g.14029014A>G GRCh38
NC_000019.9:g.14139826A>G , CM000681.1:g.14139826A>G GRCh37
NC_000019.8:g.14000826A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000431365.3:c.190+620A>G MANE Select ENSP00000397415.2:n.190+620A>G
ENST00000431365.2:c.190+620A>G ENSP00000397415.2:n.190+620A>G
ENST00000585987.1:c.190+620A>G ENSP00000467130.1:n.190+620A>G
NM_001311197.1:c.190+620A>G NP_001298126.1:n.190+620A>G
NM_080864.2:c.190+620A>G NP_543140.1:n.190+620A>G
NM_080864.3:c.190+620A>G NP_543140.1:n.190+620A>G
NM_080864.4:c.190+620A>G MANE Select NP_543140.1:n.190+620A>G
NM_001311197.2:c.190+620A>G NP_001298126.1:n.190+620A>G
Search 100 bp 5'
Search 100 bp 3'