Canonical Allele Identifier: CA2211947516
Gene: UMOD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353147A= , CM000678.2:g.20353147A= GRCh38
NC_000016.9:g.20364469A= , CM000678.1:g.20364469A= GRCh37
NC_000016.8:g.20271970A= NCBI36
NG_008151.1:g.4569T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570689.5:c.-39-2371T= ENSP00000460548.1:n.-39-2371T=
XM_011545938.1:c.-39-2371T= XP_011544240.1:n.-39-2371T=