Canonical Allele Identifier: CA35752038
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs994992696
gnomAD v3: 1-204190245-G-A
gnomAD v4: 1-204190245-G-A
MyVariant Identifiers: chr1:g.204159373G>A (hg19) chr1:g.204190245G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190245G>A , CM000663.2:g.204190245G>A GRCh38
NC_000001.10:g.204159373G>A , CM000663.1:g.204159373G>A GRCh37
NC_000001.9:g.202425996G>A NCBI36
NG_032151.1:g.11247C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638118.1:c.-224C>T ENSP00000490307.1:n.-224C>T
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