Canonical Allele Identifier: CA783524197
Gene: RLN3 HGNC NCBI

Linked Data

dbSNP Id: rs1375866425
gnomAD v3: 19-14029145-C-G
gnomAD v4: 19-14029145-C-G
MyVariant Identifiers: chr19:g.14139957C>G (hg19) chr19:g.14029145C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.14029145C>G , CM000681.2:g.14029145C>G GRCh38
NC_000019.9:g.14139957C>G , CM000681.1:g.14139957C>G GRCh37
NC_000019.8:g.14000957C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000431365.3:c.190+751C>G MANE Select ENSP00000397415.2:n.190+751C>G
ENST00000431365.2:c.190+751C>G ENSP00000397415.2:n.190+751C>G
ENST00000585987.1:c.190+751C>G ENSP00000467130.1:n.190+751C>G
NM_001311197.1:c.190+751C>G NP_001298126.1:n.190+751C>G
NM_080864.2:c.190+751C>G NP_543140.1:n.190+751C>G
NM_080864.3:c.190+751C>G NP_543140.1:n.190+751C>G
NM_080864.4:c.190+751C>G MANE Select NP_543140.1:n.190+751C>G
NM_001311197.2:c.190+751C>G NP_001298126.1:n.190+751C>G
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