Canonical Allele Identifier: CA2806171376
Gene: UMOD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353384C>T , CM000678.2:g.20353384C>T GRCh38
NC_000016.9:g.20364706C>T , CM000678.1:g.20364706C>T GRCh37
NC_000016.8:g.20272207C>T NCBI36
NG_008151.1:g.4332G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000570689.5:c.-39-2608G>A ENSP00000460548.1:n.-39-2608G>A
XM_011545938.1:c.-39-2608G>A XP_011544240.1:n.-39-2608G>A