Canonical Allele Identifier: CA35752030
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1003170164
gnomAD v3: 1-204190224-G-A
gnomAD v4: 1-204190224-G-A
MyVariant Identifiers: chr1:g.204159352G>A (hg19) chr1:g.204190224G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190224G>A , CM000663.2:g.204190224G>A GRCh38
NC_000001.10:g.204159352G>A , CM000663.1:g.204159352G>A GRCh37
NC_000001.9:g.202425975G>A NCBI36
NG_032151.1:g.11268C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638118.1:c.-211+8C>T ENSP00000490307.1:n.-211+8C>T
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