Canonical Allele Identifier: CA35752046
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs894431503
gnomAD v3: 1-204190289-G-C
gnomAD v4: 1-204190289-G-C
MyVariant Identifiers: chr1:g.204159417G>C (hg19) chr1:g.204190289G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190289G>C , CM000663.2:g.204190289G>C GRCh38
NC_000001.10:g.204159417G>C , CM000663.1:g.204159417G>C GRCh37
NC_000001.9:g.202426040G>C NCBI36
NG_032151.1:g.11203C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000638118.1:c.-268C>G ENSP00000490307.1:n.-268C>G
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