Canonical Allele Identifier: CA730306901
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1243949139
gnomAD v3: 1-204190263-C-G
gnomAD v4: 1-204190263-C-G
MyVariant Identifiers: chr1:g.204159391C>G (hg19) chr1:g.204190263C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190263C>G , CM000663.2:g.204190263C>G GRCh38
NC_000001.10:g.204159391C>G , CM000663.1:g.204159391C>G GRCh37
NC_000001.9:g.202426014C>G NCBI36
NG_032151.1:g.11229G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638118.1:c.-242G>C ENSP00000490307.1:n.-242G>C
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