Canonical Allele Identifier: CA993790938

Gene: RLN3

Linked Data

• dbSNP Id: rs1975758869
• gnomAD v3: 19-14029013-A-C
• gnomAD v4: 19-14029013-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.14029013A>C , CM000681.2:g.14029013A>C	GRCh38
NC_000019.9:g.14139825A>C , CM000681.1:g.14139825A>C	GRCh37
NC_000019.8:g.14000825A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000431365.3:c.190+619A>C MANE Select	ENSP00000397415.2:n.190+619A>C
ENST00000431365.2:c.190+619A>C	ENSP00000397415.2:n.190+619A>C
ENST00000585987.1:c.190+619A>C	ENSP00000467130.1:n.190+619A>C
NM_001311197.1:c.190+619A>C	NP_001298126.1:n.190+619A>C
NM_080864.2:c.190+619A>C	NP_543140.1:n.190+619A>C
NM_080864.3:c.190+619A>C	NP_543140.1:n.190+619A>C
NM_080864.4:c.190+619A>C MANE Select	NP_543140.1:n.190+619A>C
NM_001311197.2:c.190+619A>C	NP_001298126.1:n.190+619A>C