Canonical Allele Identifier: CA2211947638
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs1965972844
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353382G>T , CM000678.2:g.20353382G>T GRCh38
NC_000016.9:g.20364704G>T , CM000678.1:g.20364704G>T GRCh37
NC_000016.8:g.20272205G>T NCBI36
NG_008151.1:g.4334C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000570689.5:c.-39-2606C>A ENSP00000460548.1:n.-39-2606C>A
XM_011545938.1:c.-39-2606C>A XP_011544240.1:n.-39-2606C>A
Search 100 bp 5'
Search 100 bp 3'