Canonical Allele Identifier: CA32388558

Gene: F5

Linked Data

• dbSNP Id: rs182367565
• MyVariant Identifiers: chr1:g.169521528C>A (hg19) ; chr1:g.169552290C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552290C>A , CM000663.2:g.169552290C>A	GRCh38
NC_000001.10:g.169521528C>A , CM000663.1:g.169521528C>A	GRCh37
NC_000001.9:g.167788152C>A	NCBI36
NG_011806.1:g.39242G>T , LRG_553:g.39242G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1296+267G>T MANE Select	ENSP00000356771.3:n.1296+267G>T
ENST00000367796.3:c.1296+267G>T	ENSP00000356770.3:n.1296+267G>T
ENST00000367797.7:c.1296+267G>T	ENSP00000356771.3:n.1296+267G>T
NM_000130.4:c.1296+267G>T , LRG_553t1:c.1296+267G>T	NP_000121.2:n.1296+267G>T
XM_017000660.2:c.885+267G>T	XP_016856149.1:n.885+267G>T
NM_000130.5:c.1296+267G>T MANE Select	NP_000121.2:n.1296+267G>T