Canonical Allele Identifier: CA35734610
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1023661590
MyVariant Identifiers: chr1:g.204128682C>A (hg19) chr1:g.204159554C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159554C>A , CM000663.2:g.204159554C>A GRCh38
NC_000001.10:g.204128682C>A , CM000663.1:g.204128682C>A GRCh37
NC_000001.9:g.202395305C>A NCBI36
NG_012122.1:g.11784G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.534G>T MANE Select ENSP00000272190.8:p.Thr178=
ENST00000638118.1:c.420G>T ENSP00000490307.1:p.Thr140=
ENST00000272190.8:c.534G>T ENSP00000272190.8:p.Thr178=
NM_000537.3:c.534G>T NP_000528.1:p.Thr178=
NM_000537.4:c.534G>T MANE Select NP_000528.1:p.Thr178=
Search 100 bp 5'
Search 100 bp 3'