Canonical Allele Identifier: CA718913220
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs1315130446
gnomAD v3: 16-20353363-C-T
gnomAD v4: 16-20353363-C-T
MyVariant Identifiers: chr16:g.20364685C>T (hg19) chr16:g.20353363C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353363C>T , CM000678.2:g.20353363C>T GRCh38
NC_000016.9:g.20364685C>T , CM000678.1:g.20364685C>T GRCh37
NC_000016.8:g.20272186C>T NCBI36
NG_008151.1:g.4353G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000570689.5:c.-39-2587G>A ENSP00000460548.1:n.-39-2587G>A
XM_011545938.1:c.-39-2587G>A XP_011544240.1:n.-39-2587G>A
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