Canonical Allele Identifier: CA422837320
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128535G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159407G>A , CM000663.2:g.204159407G>A GRCh38
NC_000001.10:g.204128535G>A , CM000663.1:g.204128535G>A GRCh37
NC_000001.9:g.202395158G>A NCBI36
NG_012122.1:g.11931C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.681C>T MANE Select ENSP00000272190.8:p.Tyr227=
ENST00000638118.1:c.567C>T ENSP00000490307.1:p.Tyr189=
ENST00000272190.8:c.681C>T ENSP00000272190.8:p.Tyr227=
NM_000537.3:c.681C>T NP_000528.1:p.Tyr227=
NM_000537.4:c.681C>T MANE Select NP_000528.1:p.Tyr227=
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