Canonical Allele Identifier: CA422840582
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1658347720
MyVariant Identifiers: chr1:g.204135386C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204166258C>A , CM000663.2:g.204166258C>A GRCh38
NC_000001.10:g.204135386C>A , CM000663.1:g.204135386C>A GRCh37
NC_000001.9:g.202402009C>A NCBI36
NG_012122.1:g.5080G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.36G>T MANE Select ENSP00000272190.8:p.Leu12=
ENST00000638118.1:c.-16-4095G>T ENSP00000490307.1:n.-16-4095G>T
ENST00000272190.8:c.36G>T ENSP00000272190.8:p.Leu12=
NM_000537.3:c.36G>T NP_000528.1:p.Leu12=
NM_000537.4:c.36G>T MANE Select NP_000528.1:p.Leu12=
Search 100 bp 5'
Search 100 bp 3'