Canonical Allele Identifier: CA2211947582
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs1965971112

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353264T>C , CM000678.2:g.20353264T>C GRCh38
NC_000016.9:g.20364586T>C , CM000678.1:g.20364586T>C GRCh37
NC_000016.8:g.20272087T>C NCBI36
NG_008151.1:g.4452A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000570689.5:c.-39-2488A>G ENSP00000460548.1:n.-39-2488A>G
XM_011545938.1:c.-39-2488A>G XP_011544240.1:n.-39-2488A>G