Canonical Allele Identifier: CA305606145
Gene: RLN3 HGNC NCBI

Linked Data

dbSNP Id: rs781548157
MyVariant Identifiers: chr19:g.14139827G>C (hg19) chr19:g.14029015G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.14029015G>C , CM000681.2:g.14029015G>C GRCh38
NC_000019.9:g.14139827G>C , CM000681.1:g.14139827G>C GRCh37
NC_000019.8:g.14000827G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000431365.3:c.190+621G>C MANE Select ENSP00000397415.2:n.190+621G>C
ENST00000431365.2:c.190+621G>C ENSP00000397415.2:n.190+621G>C
ENST00000585987.1:c.190+621G>C ENSP00000467130.1:n.190+621G>C
NM_001311197.1:c.190+621G>C NP_001298126.1:n.190+621G>C
NM_080864.2:c.190+621G>C NP_543140.1:n.190+621G>C
NM_080864.3:c.190+621G>C NP_543140.1:n.190+621G>C
NM_080864.4:c.190+621G>C MANE Select NP_543140.1:n.190+621G>C
NM_001311197.2:c.190+621G>C NP_001298126.1:n.190+621G>C
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