Canonical Allele Identifier: CA16520535
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs4293393

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353266A>G , CM000678.2:g.20353266A>G GRCh38
NC_000016.9:g.20364588A>G , CM000678.1:g.20364588A>G GRCh37
NC_000016.8:g.20272089A>G NCBI36
NG_008151.1:g.4450T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000570689.5:c.-39-2490T>C ENSP00000460548.1:p.=
XM_011545938.1:c.-39-2490T>C XP_011544240.1:p.=