Canonical Allele Identifier: CA2211947548
Gene: UMOD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353194T= , CM000678.2:g.20353194T= GRCh38
NC_000016.9:g.20364516T= , CM000678.1:g.20364516T= GRCh37
NC_000016.8:g.20272017T= NCBI36
NG_008151.1:g.4522A=

Transcript Alleles

HGVS Amino-acid change
ENST00000570689.5:c.-39-2418A= ENSP00000460548.1:n.-39-2418A=
XM_011545938.1:c.-39-2418A= XP_011544240.1:n.-39-2418A=