Canonical Allele Identifier: CA344342006
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204131249C>A (hg19) chr1:g.204162121C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204162121C>A , CM000663.2:g.204162121C>A GRCh38
NC_000001.10:g.204131249C>A , CM000663.1:g.204131249C>A GRCh37
NC_000001.9:g.202397872C>A NCBI36
NG_012122.1:g.9217G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.141G>T MANE Select ENSP00000272190.8:p.Lys47Asn
ENST00000638118.1:c.27G>T ENSP00000490307.1:p.Lys9Asn
ENST00000272190.8:c.141G>T ENSP00000272190.8:p.Lys47Asn
NM_000537.3:c.141G>T NP_000528.1:p.Lys47Asn
NM_000537.4:c.141G>T MANE Select NP_000528.1:p.Lys47Asn
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