Canonical Allele Identifier: CA2211947510
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs1965968030
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353141A>C , CM000678.2:g.20353141A>C GRCh38
NC_000016.9:g.20364463A>C , CM000678.1:g.20364463A>C GRCh37
NC_000016.8:g.20271964A>C NCBI36
NG_008151.1:g.4575T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000570689.5:c.-39-2365T>G ENSP00000460548.1:n.-39-2365T>G
XM_011545938.1:c.-39-2365T>G XP_011544240.1:n.-39-2365T>G
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