Canonical Allele Identifier: CA2211947567
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs1965970114

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353218C>A , CM000678.2:g.20353218C>A GRCh38
NC_000016.9:g.20364540C>A , CM000678.1:g.20364540C>A GRCh37
NC_000016.8:g.20272041C>A NCBI36
NG_008151.1:g.4498G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000570689.5:c.-39-2442G>T ENSP00000460548.1:n.-39-2442G>T
XM_011545938.1:c.-39-2442G>T XP_011544240.1:n.-39-2442G>T