Canonical Allele Identifier: CA32390522

Gene: F5

Linked Data

• dbSNP Id: rs972906246
• gnomAD v4: 1-169555134-G-A
• MyVariant Identifiers: chr1:g.169524372G>A (hg19) ; chr1:g.169555134G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555134G>A , CM000663.2:g.169555134G>A	GRCh38
NC_000001.10:g.169524372G>A , CM000663.1:g.169524372G>A	GRCh37
NC_000001.9:g.167790996G>A	NCBI36
NG_011806.1:g.36398C>T , LRG_553:g.36398C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1118+48C>T MANE Select	ENSP00000356771.3:n.1118+48C>T
ENST00000367796.3:c.1118+48C>T	ENSP00000356770.3:n.1118+48C>T
ENST00000367797.7:c.1118+48C>T	ENSP00000356771.3:n.1118+48C>T
NM_000130.4:c.1118+48C>T , LRG_553t1:c.1118+48C>T	NP_000121.2:n.1118+48C>T
XM_017000660.2:c.707+48C>T	XP_016856149.1:n.707+48C>T
NM_000130.5:c.1118+48C>T MANE Select	NP_000121.2:n.1118+48C>T