Canonical Allele Identifier: CA2211947490
Gene: UMOD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353091T= , CM000678.2:g.20353091T= GRCh38
NC_000016.9:g.20364413T= , CM000678.1:g.20364413T= GRCh37
NC_000016.8:g.20271914T= NCBI36
NG_008151.1:g.4625A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570689.5:c.-39-2315A= ENSP00000460548.1:n.-39-2315A=
XM_011545938.1:c.-39-2315A= XP_011544240.1:n.-39-2315A=