Canonical Allele Identifier: CA279253462
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs1044066386
MyVariant Identifiers: chr16:g.20364436A>G (hg19) chr16:g.20353114A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353114A>G , CM000678.2:g.20353114A>G GRCh38
NC_000016.9:g.20364436A>G , CM000678.1:g.20364436A>G GRCh37
NC_000016.8:g.20271937A>G NCBI36
NG_008151.1:g.4602T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000570689.5:c.-39-2338T>C ENSP00000460548.1:n.-39-2338T>C
XM_011545938.1:c.-39-2338T>C XP_011544240.1:n.-39-2338T>C
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