Canonical Allele Identifier: CA2672900954

Gene: F11

Linked Data

• gnomAD v4: 4-186265957-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186265957G>T , CM000666.2:g.186265957G>T	GRCh38
NC_000004.11:g.187187111G>T , CM000666.1:g.187187111G>T	GRCh37
NC_000004.10:g.187424105G>T	NCBI36
NG_008051.1:g.4994G>T , LRG_583:g.4994G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.6:c.-340G>T	ENSP00000384957.2:n.-340G>T
XM_005262821.2:c.-340G>T	XP_005262878.1:n.-340G>T
XM_005262822.2:c.-340G>T	XP_005262879.1:n.-340G>T
XM_005262823.2:c.-340G>T	XP_005262880.1:n.-340G>T
XM_005262824.1:c.-340G>T	XP_005262881.1:n.-340G>T
XM_006714137.1:c.-340G>T	XP_006714200.1:n.-340G>T
XR_938706.1:n.13G>T
XR_938707.1:n.13G>T