Canonical Allele Identifier: CA2613335443

Gene: F2

Linked Data

• gnomAD v4: 11-46727858-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46727858C>T , CM000673.2:g.46727858C>T	GRCh38
NC_000011.9:g.46749408C>T , CM000673.1:g.46749408C>T	GRCh37
NC_000011.8:g.46705984C>T	NCBI36
NG_008953.1:g.13666C>T , LRG_551:g.13666C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1131-138C>T MANE Select	ENSP00000308541.5:n.1131-138C>T
ENST00000311907.9:c.1131-138C>T	ENSP00000308541.5:n.1131-138C>T
ENST00000530231.5:c.1131-138C>T	ENSP00000433907.1:n.1131-138C>T
NM_000506.3:c.1131-138C>T	NP_000497.1:n.1131-138C>T
NM_000506.4:c.1131-138C>T , LRG_551t1:c.1131-138C>T	NP_000497.1:n.1131-138C>T
NM_001311257.1:c.1083-138C>T	NP_001298186.1:n.1083-138C>T
XR_428840.2:n.1175-138C>T
XR_428840.4:n.1166-138C>T
NM_000506.5:c.1131-138C>T MANE Select	NP_000497.1:n.1131-138C>T
NM_001311257.2:c.1083-138C>T	NP_001298186.1:n.1083-138C>T