Canonical Allele Identifier: CA2672900953

Gene: F11

Linked Data

• gnomAD v4: 4-186265953-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186265953C>A , CM000666.2:g.186265953C>A	GRCh38
NC_000004.11:g.187187107C>A , CM000666.1:g.187187107C>A	GRCh37
NC_000004.10:g.187424101C>A	NCBI36
NG_008051.1:g.4990C>A , LRG_583:g.4990C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.6:c.-344C>A	ENSP00000384957.2:n.-344C>A
XM_005262821.2:c.-344C>A	XP_005262878.1:n.-344C>A
XM_005262822.2:c.-344C>A	XP_005262879.1:n.-344C>A
XM_005262823.2:c.-344C>A	XP_005262880.1:n.-344C>A
XM_005262824.1:c.-344C>A	XP_005262881.1:n.-344C>A
XM_006714137.1:c.-344C>A	XP_006714200.1:n.-344C>A
XR_938706.1:n.9C>A
XR_938707.1:n.9C>A