Canonical Allele Identifier: CA2613334823

Gene: F2

Linked Data

• gnomAD v4: 11-46726222-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726222G>T , CM000673.2:g.46726222G>T	GRCh38
NC_000011.9:g.46747772G>T , CM000673.1:g.46747772G>T	GRCh37
NC_000011.8:g.46704348G>T	NCBI36
NG_008953.1:g.12030G>T , LRG_551:g.12030G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+49G>T MANE Select	ENSP00000308541.5:n.874+49G>T
ENST00000311907.9:c.874+49G>T	ENSP00000308541.5:n.874+49G>T
ENST00000442468.1:c.844+49G>T	ENSP00000387413.1:n.844+49G>T
ENST00000530231.5:c.874+49G>T	ENSP00000433907.1:n.874+49G>T
NM_000506.3:c.874+49G>T	NP_000497.1:n.874+49G>T
NM_000506.4:c.874+49G>T , LRG_551t1:c.874+49G>T	NP_000497.1:n.874+49G>T
NM_001311257.1:c.826+49G>T	NP_001298186.1:n.826+49G>T
XR_428840.2:n.918+49G>T
XR_428840.4:n.909+49G>T
NM_000506.5:c.874+49G>T MANE Select	NP_000497.1:n.874+49G>T
NM_001311257.2:c.826+49G>T	NP_001298186.1:n.826+49G>T