Canonical Allele Identifier: CA344342159
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204131292C>A (hg19) chr1:g.204162164C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204162164C>A , CM000663.2:g.204162164C>A GRCh38
NC_000001.10:g.204131292C>A , CM000663.1:g.204131292C>A GRCh37
NC_000001.9:g.202397915C>A NCBI36
NG_012122.1:g.9174G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.99-1G>T MANE Select ENSP00000272190.8:n.99-1G>T
ENST00000638118.1:c.-16-1G>T ENSP00000490307.1:n.-16-1G>T
ENST00000272190.8:c.99-1G>T ENSP00000272190.8:n.99-1G>T
NM_000537.3:c.99-1G>T NP_000528.1:n.99-1G>T
NM_000537.4:c.99-1G>T MANE Select NP_000528.1:n.99-1G>T
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