Canonical Allele Identifier: CA35752047
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs995122932
gnomAD v4: 1-204190291-A-G
MyVariant Identifiers: chr1:g.204159419A>G (hg19) chr1:g.204190291A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190291A>G , CM000663.2:g.204190291A>G GRCh38
NC_000001.10:g.204159419A>G , CM000663.1:g.204159419A>G GRCh37
NC_000001.9:g.202426042A>G NCBI36
NG_032151.1:g.11201T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638118.1:c.-270T>C ENSP00000490307.1:n.-270T>C
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