Canonical Allele Identifier: CA1234464

Gene: F5

Linked Data

• dbSNP Id: rs541800681
• ExAC: 1:169524595 G / A
• gnomAD v2: 1-169524595-G-A
• gnomAD v3: 1-169555357-G-A
• gnomAD v4: 1-169555357-G-A
• MyVariant Identifiers: chr1:g.169524595G>A (hg19) ; chr1:g.169555357G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555357G>A , CM000663.2:g.169555357G>A	GRCh38
NC_000001.10:g.169524595G>A , CM000663.1:g.169524595G>A	GRCh37
NC_000001.9:g.167791219G>A	NCBI36
NG_011806.1:g.36175C>T , LRG_553:g.36175C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.953-10C>T MANE Select	ENSP00000356771.3:n.953-10C>T
ENST00000367796.3:c.953-10C>T	ENSP00000356770.3:n.953-10C>T
ENST00000367797.7:c.953-10C>T	ENSP00000356771.3:n.953-10C>T
NM_000130.4:c.953-10C>T , LRG_553t1:c.953-10C>T	NP_000121.2:n.953-10C>T
XM_017000660.2:c.542-10C>T	XP_016856149.1:n.542-10C>T
NM_000130.5:c.953-10C>T MANE Select	NP_000121.2:n.953-10C>T