Canonical Allele Identifier: CA528532067
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1372585009
gnomAD v2: 1-204124116-G-A
gnomAD v4: 1-204154988-G-A
MyVariant Identifiers: chr1:g.204124116G>A (hg19) chr1:g.204154988G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204154988G>A , CM000663.2:g.204154988G>A GRCh38
NC_000001.10:g.204124116G>A , CM000663.1:g.204124116G>A GRCh37
NC_000001.9:g.202390739G>A NCBI36
NG_012122.1:g.16350C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.*28C>T MANE Select ENSP00000272190.8:n.*28C>T
ENST00000638118.1:c.*28C>T ENSP00000490307.1:n.*28C>T
ENST00000272190.8:c.*28C>T ENSP00000272190.8:n.*28C>T
NM_000537.3:c.*28C>T NP_000528.1:n.*28C>T
NM_000537.4:c.*28C>T MANE Select NP_000528.1:n.*28C>T
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