Canonical Allele Identifier: CA2613335691

Gene: F2

Linked Data

• gnomAD v4: 11-46728229-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728229C>A , CM000673.2:g.46728229C>A	GRCh38
NC_000011.9:g.46749779C>A , CM000673.1:g.46749779C>A	GRCh37
NC_000011.8:g.46706355C>A	NCBI36
NG_008953.1:g.14037C>A , LRG_551:g.14037C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1298+66C>A MANE Select	ENSP00000308541.5:n.1298+66C>A
ENST00000311907.9:c.1298+66C>A	ENSP00000308541.5:n.1298+66C>A
ENST00000530231.5:c.1298+66C>A	ENSP00000433907.1:n.1298+66C>A
NM_000506.3:c.1298+66C>A	NP_000497.1:n.1298+66C>A
NM_000506.4:c.1298+66C>A , LRG_551t1:c.1298+66C>A	NP_000497.1:n.1298+66C>A
NM_001311257.1:c.1250+66C>A	NP_001298186.1:n.1250+66C>A
XR_428840.2:n.1342+66C>A
XR_428840.4:n.1333+66C>A
NM_000506.5:c.1298+66C>A MANE Select	NP_000497.1:n.1298+66C>A
NM_001311257.2:c.1250+66C>A	NP_001298186.1:n.1250+66C>A