Canonical Allele Identifier: CA422837541
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1658207993
MyVariant Identifiers: chr1:g.204128721C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159593C>T , CM000663.2:g.204159593C>T GRCh38
NC_000001.10:g.204128721C>T , CM000663.1:g.204128721C>T GRCh37
NC_000001.9:g.202395344C>T NCBI36
NG_012122.1:g.11745G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.495G>A MANE Select ENSP00000272190.8:p.Val165=
ENST00000638118.1:c.381G>A ENSP00000490307.1:p.Val127=
ENST00000272190.8:c.495G>A ENSP00000272190.8:p.Val165=
NM_000537.3:c.495G>A NP_000528.1:p.Val165=
NM_000537.4:c.495G>A MANE Select NP_000528.1:p.Val165=
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Search 100 bp 3'