Canonical Allele Identifier: CA1234376

Gene: F5

Linked Data

• dbSNP Id: rs376636380
• ExAC: 1:169521771 T / G
• gnomAD v2: 1-169521771-T-G
• gnomAD v3: 1-169552533-T-G
• gnomAD v4: 1-169552533-T-G
• MyVariant Identifiers: chr1:g.169521771T>G (hg19) ; chr1:g.169552533T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552533T>G , CM000663.2:g.169552533T>G	GRCh38
NC_000001.10:g.169521771T>G , CM000663.1:g.169521771T>G	GRCh37
NC_000001.9:g.167788395T>G	NCBI36
NG_011806.1:g.38999A>C , LRG_553:g.38999A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1296+24A>C MANE Select	ENSP00000356771.3:n.1296+24A>C
ENST00000367796.3:c.1296+24A>C	ENSP00000356770.3:n.1296+24A>C
ENST00000367797.7:c.1296+24A>C	ENSP00000356771.3:n.1296+24A>C
NM_000130.4:c.1296+24A>C , LRG_553t1:c.1296+24A>C	NP_000121.2:n.1296+24A>C
XM_017000660.2:c.885+24A>C	XP_016856149.1:n.885+24A>C
NM_000130.5:c.1296+24A>C MANE Select	NP_000121.2:n.1296+24A>C