Canonical Allele Identifier: CA1008977140

Gene: F5

Linked Data

• dbSNP Id: rs1660115661
• gnomAD v3: 1-169549742-A-G
• gnomAD v4: 1-169549742-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549742A>G , CM000663.2:g.169549742A>G	GRCh38
NC_000001.10:g.169518980A>G , CM000663.1:g.169518980A>G	GRCh37
NC_000001.9:g.167785604A>G	NCBI36
NG_011806.1:g.41790T>C , LRG_553:g.41790T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.1611+59T>C MANE Select	ENSP00000356771.3:n.1611+59T>C
ENST00000367796.3:c.1611+59T>C	ENSP00000356770.3:n.1611+59T>C
ENST00000367797.7:c.1611+59T>C	ENSP00000356771.3:n.1611+59T>C
NM_000130.4:c.1611+59T>C , LRG_553t1:c.1611+59T>C	NP_000121.2:n.1611+59T>C
XM_017000660.2:c.1200+59T>C	XP_016856149.1:n.1200+59T>C
NM_000130.5:c.1611+59T>C MANE Select	NP_000121.2:n.1611+59T>C