Canonical Allele Identifier: CA2211947517
Gene: UMOD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353148C= , CM000678.2:g.20353148C= GRCh38
NC_000016.9:g.20364470C= , CM000678.1:g.20364470C= GRCh37
NC_000016.8:g.20271971C= NCBI36
NG_008151.1:g.4568G=

Transcript Alleles

HGVS Amino-acid change
ENST00000570689.5:c.-39-2372G= ENSP00000460548.1:n.-39-2372G=
XM_011545938.1:c.-39-2372G= XP_011544240.1:n.-39-2372G=