Canonical Allele Identifier: CA2211947529
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs1965968756
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353162G>T , CM000678.2:g.20353162G>T GRCh38
NC_000016.9:g.20364484G>T , CM000678.1:g.20364484G>T GRCh37
NC_000016.8:g.20271985G>T NCBI36
NG_008151.1:g.4554C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000570689.5:c.-39-2386C>A ENSP00000460548.1:n.-39-2386C>A
XM_011545938.1:c.-39-2386C>A XP_011544240.1:n.-39-2386C>A
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