Canonical Allele Identifier: CA2806171372
Gene: UMOD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353247C>A , CM000678.2:g.20353247C>A GRCh38
NC_000016.9:g.20364569C>A , CM000678.1:g.20364569C>A GRCh37
NC_000016.8:g.20272070C>A NCBI36
NG_008151.1:g.4469G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000570689.5:c.-39-2471G>T ENSP00000460548.1:n.-39-2471G>T
XM_011545938.1:c.-39-2471G>T XP_011544240.1:n.-39-2471G>T
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