Canonical Allele Identifier: CA2708191204

Gene: F11

Linked Data

• dbSNP Id: rs2126695671

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186265947A>C , CM000666.2:g.186265947A>C	GRCh38
NC_000004.11:g.187187101A>C , CM000666.1:g.187187101A>C	GRCh37
NC_000004.10:g.187424095A>C	NCBI36
NG_008051.1:g.4984A>C , LRG_583:g.4984A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.6:c.-350A>C	ENSP00000384957.2:n.-350A>C
XM_005262821.2:c.-350A>C	XP_005262878.1:n.-350A>C
XM_005262822.2:c.-350A>C	XP_005262879.1:n.-350A>C
XM_005262823.2:c.-350A>C	XP_005262880.1:n.-350A>C
XM_005262824.1:c.-350A>C	XP_005262881.1:n.-350A>C
XM_006714137.1:c.-350A>C	XP_006714200.1:n.-350A>C
XR_938706.1:n.3A>C
XR_938707.1:n.3A>C