Canonical Allele Identifier: CA421930522

Gene: F5

Linked Data

• gnomAD v4: 1-169541721-T-G
• MyVariant Identifiers: chr1:g.169510959T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541721T>G , CM000663.2:g.169541721T>G	GRCh38
NC_000001.10:g.169510959T>G , CM000663.1:g.169510959T>G	GRCh37
NC_000001.9:g.167777583T>G	NCBI36
NG_011806.1:g.49811A>C , LRG_553:g.49811A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3369A>C MANE Select	ENSP00000356771.3:p.Pro1123=
ENST00000367796.3:c.3384A>C	ENSP00000356770.3:p.Pro1128=
ENST00000367797.7:c.3369A>C	ENSP00000356771.3:p.Pro1123=
NM_000130.4:c.3369A>C , LRG_553t1:c.3369A>C	NP_000121.2:p.Pro1123=
XM_017000660.2:c.2958A>C	XP_016856149.1:p.Pro986=
NM_000130.5:c.3369A>C MANE Select	NP_000121.2:p.Pro1123=