Canonical Allele Identifier: CA344337984
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204128597T>A (hg19) chr1:g.204159469T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159469T>A , CM000663.2:g.204159469T>A GRCh38
NC_000001.10:g.204128597T>A , CM000663.1:g.204128597T>A GRCh37
NC_000001.9:g.202395220T>A NCBI36
NG_012122.1:g.11869A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.619A>T MANE Select ENSP00000272190.8:p.Thr207Ser
ENST00000638118.1:c.505A>T ENSP00000490307.1:p.Thr169Ser
ENST00000272190.8:c.619A>T ENSP00000272190.8:p.Thr207Ser
NM_000537.3:c.619A>T NP_000528.1:p.Thr207Ser
NM_000537.4:c.619A>T MANE Select NP_000528.1:p.Thr207Ser
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