Canonical Allele Identifier: CA1011402128
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1658325316
gnomAD v3: 1-204165350-T-C
gnomAD v4: 1-204165350-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165350T>C , CM000663.2:g.204165350T>C GRCh38
NC_000001.10:g.204134478T>C , CM000663.1:g.204134478T>C GRCh37
NC_000001.9:g.202401101T>C NCBI36
NG_012122.1:g.5988A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.98+846A>G MANE Select ENSP00000272190.8:n.98+846A>G
ENST00000638118.1:c.-16-3187A>G ENSP00000490307.1:n.-16-3187A>G
ENST00000272190.8:c.98+846A>G ENSP00000272190.8:n.98+846A>G
NM_000537.3:c.98+846A>G NP_000528.1:n.98+846A>G
NM_000537.4:c.98+846A>G MANE Select NP_000528.1:n.98+846A>G
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