Canonical Allele Identifier: CA718913134
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs1244351109
gnomAD v3: 16-20353148-C-T
gnomAD v4: 16-20353148-C-T
MyVariant Identifiers: chr16:g.20364470C>T (hg19) chr16:g.20353148C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353148C>T , CM000678.2:g.20353148C>T GRCh38
NC_000016.9:g.20364470C>T , CM000678.1:g.20364470C>T GRCh37
NC_000016.8:g.20271971C>T NCBI36
NG_008151.1:g.4568G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000570689.5:c.-39-2372G>A ENSP00000460548.1:n.-39-2372G>A
XM_011545938.1:c.-39-2372G>A XP_011544240.1:n.-39-2372G>A
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