Canonical Allele Identifier: CA783524192
Gene: RLN3 HGNC NCBI

Linked Data

dbSNP Id: rs1245158182
gnomAD v3: 19-14029144-G-A
gnomAD v4: 19-14029144-G-A
MyVariant Identifiers: chr19:g.14139956G>A (hg19) chr19:g.14029144G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.14029144G>A , CM000681.2:g.14029144G>A GRCh38
NC_000019.9:g.14139956G>A , CM000681.1:g.14139956G>A GRCh37
NC_000019.8:g.14000956G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000431365.3:c.190+750G>A MANE Select ENSP00000397415.2:n.190+750G>A
ENST00000431365.2:c.190+750G>A ENSP00000397415.2:n.190+750G>A
ENST00000585987.1:c.190+750G>A ENSP00000467130.1:n.190+750G>A
NM_001311197.1:c.190+750G>A NP_001298126.1:n.190+750G>A
NM_080864.2:c.190+750G>A NP_543140.1:n.190+750G>A
NM_080864.3:c.190+750G>A NP_543140.1:n.190+750G>A
NM_080864.4:c.190+750G>A MANE Select NP_543140.1:n.190+750G>A
NM_001311197.2:c.190+750G>A NP_001298126.1:n.190+750G>A
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