Canonical Allele Identifier: CA975446587
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs1965971003
gnomAD v3: 16-20353262-G-A
gnomAD v4: 16-20353262-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353262G>A , CM000678.2:g.20353262G>A GRCh38
NC_000016.9:g.20364584G>A , CM000678.1:g.20364584G>A GRCh37
NC_000016.8:g.20272085G>A NCBI36
NG_008151.1:g.4454C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000570689.5:c.-39-2486C>T ENSP00000460548.1:n.-39-2486C>T
XM_011545938.1:c.-39-2486C>T XP_011544240.1:n.-39-2486C>T
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