Canonical Allele Identifier: CA35752032
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs945504152
gnomAD v3: 1-204190228-T-G
gnomAD v4: 1-204190228-T-G
MyVariant Identifiers: chr1:g.204159356T>G (hg19) chr1:g.204190228T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190228T>G , CM000663.2:g.204190228T>G GRCh38
NC_000001.10:g.204159356T>G , CM000663.1:g.204159356T>G GRCh37
NC_000001.9:g.202425979T>G NCBI36
NG_032151.1:g.11264A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638118.1:c.-211+4A>C ENSP00000490307.1:n.-211+4A>C
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