Canonical Allele Identifier: CA32418337

Gene: F5

Linked Data

• dbSNP Id: rs766753985
• gnomAD v4: 1-169586626-G-A
• MyVariant Identifiers: chr1:g.169555864G>A (hg19) ; chr1:g.169586626G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169586626G>A , CM000663.2:g.169586626G>A	GRCh38
NC_000001.10:g.169555864G>A , CM000663.1:g.169555864G>A	GRCh37
NC_000001.9:g.167822488G>A	NCBI36
NG_011806.1:g.4906C>T , LRG_553:g.4906C>T

Transcript Alleles

HGVS	Amino-acid Change
XM_017000660.2:c.-559C>T	XP_016856149.1:n.-559C>T