Canonical Allele Identifier: CA1344665
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs374392027
ExAC: 1:204124331 C / T
gnomAD v2: 1-204124331-C-T
gnomAD v3: 1-204155203-C-T
gnomAD v4: 1-204155203-C-T
MyVariant Identifiers: chr1:g.204124331C>T (hg19) chr1:g.204155203C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155203C>T , CM000663.2:g.204155203C>T GRCh38
NC_000001.10:g.204124331C>T , CM000663.1:g.204124331C>T GRCh37
NC_000001.9:g.202390954C>T NCBI36
NG_012122.1:g.16135G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.1060-26G>A MANE Select ENSP00000272190.8:n.1060-26G>A
ENST00000638118.1:c.946-26G>A ENSP00000490307.1:n.946-26G>A
ENST00000272190.8:c.1060-26G>A ENSP00000272190.8:n.1060-26G>A
NM_000537.3:c.1060-26G>A NP_000528.1:n.1060-26G>A
NM_000537.4:c.1060-26G>A MANE Select NP_000528.1:n.1060-26G>A
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