Canonical Allele Identifier: CA730343309
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1426370961
MyVariant Identifiers: chr1:g.204134550T>C (hg19) chr1:g.204165422T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165422T>C , CM000663.2:g.204165422T>C GRCh38
NC_000001.10:g.204134550T>C , CM000663.1:g.204134550T>C GRCh37
NC_000001.9:g.202401173T>C NCBI36
NG_012122.1:g.5916A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.98+774A>G MANE Select ENSP00000272190.8:n.98+774A>G
ENST00000638118.1:c.-16-3259A>G ENSP00000490307.1:n.-16-3259A>G
ENST00000272190.8:c.98+774A>G ENSP00000272190.8:n.98+774A>G
NM_000537.3:c.98+774A>G NP_000528.1:n.98+774A>G
NM_000537.4:c.98+774A>G MANE Select NP_000528.1:n.98+774A>G
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