Canonical Allele Identifier: CA2324179167
Gene: RLN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.14029158G= , CM000681.2:g.14029158G= GRCh38
NC_000019.9:g.14139970G= , CM000681.1:g.14139970G= GRCh37
NC_000019.8:g.14000970G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000431365.3:c.190+764G= MANE Select ENSP00000397415.2:n.190+764G=
ENST00000431365.2:c.190+764G= ENSP00000397415.2:n.190+764G=
ENST00000585987.1:c.190+764G= ENSP00000467130.1:n.190+764G=
NM_001311197.1:c.190+764G= NP_001298126.1:n.190+764G=
NM_080864.2:c.190+764G= NP_543140.1:n.190+764G=
NM_080864.3:c.190+764G= NP_543140.1:n.190+764G=
NM_080864.4:c.190+764G= MANE Select NP_543140.1:n.190+764G=
NM_001311197.2:c.190+764G= NP_001298126.1:n.190+764G=