Canonical Allele Identifier: CA2211947581
Gene: UMOD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353262G= , CM000678.2:g.20353262G= GRCh38
NC_000016.9:g.20364584G= , CM000678.1:g.20364584G= GRCh37
NC_000016.8:g.20272085G= NCBI36
NG_008151.1:g.4454C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570689.5:c.-39-2486C= ENSP00000460548.1:n.-39-2486C=
XM_011545938.1:c.-39-2486C= XP_011544240.1:n.-39-2486C=