Canonical Allele Identifier: CA730306904
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1272311307
gnomAD v3: 1-204190295-C-T
gnomAD v4: 1-204190295-C-T
MyVariant Identifiers: chr1:g.204159423C>T (hg19) chr1:g.204190295C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190295C>T , CM000663.2:g.204190295C>T GRCh38
NC_000001.10:g.204159423C>T , CM000663.1:g.204159423C>T GRCh37
NC_000001.9:g.202426046C>T NCBI36
NG_032151.1:g.11197G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000638118.1:c.-274G>A ENSP00000490307.1:n.-274G>A
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