Canonical Allele Identifier: CA279253470
Gene: UMOD HGNC NCBI

Linked Data

dbSNP Id: rs905533563
gnomAD v3: 16-20353142-G-A
gnomAD v4: 16-20353142-G-A
MyVariant Identifiers: chr16:g.20364464G>A (hg19) chr16:g.20353142G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20353142G>A , CM000678.2:g.20353142G>A GRCh38
NC_000016.9:g.20364464G>A , CM000678.1:g.20364464G>A GRCh37
NC_000016.8:g.20271965G>A NCBI36
NG_008151.1:g.4574C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000570689.5:c.-39-2366C>T ENSP00000460548.1:n.-39-2366C>T
XM_011545938.1:c.-39-2366C>T XP_011544240.1:n.-39-2366C>T
Search 100 bp 5'
Search 100 bp 3'