Canonical Allele Identifier: CA718913125

Gene: UMOD

Linked Data

• dbSNP Id: rs1412272243
• MyVariant Identifiers: chr16:g.20364429A>G (hg19) ; chr16:g.20353107A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20353107A>G , CM000678.2:g.20353107A>G	GRCh38
NC_000016.9:g.20364429A>G , CM000678.1:g.20364429A>G	GRCh37
NC_000016.8:g.20271930A>G	NCBI36
NG_008151.1:g.4609T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570689.5:c.-39-2331T>C	ENSP00000460548.1:n.-39-2331T>C
XM_011545938.1:c.-39-2331T>C	XP_011544240.1:n.-39-2331T>C