Canonical Allele Identifier: CA2708189591

Gene: F11

Linked Data

• dbSNP Id: rs2126737877

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186275774T>C , CM000666.2:g.186275774T>C	GRCh38
NC_000004.11:g.187196928T>C , CM000666.1:g.187196928T>C	GRCh37
NC_000004.10:g.187433922T>C	NCBI36
NG_008051.1:g.14811T>C , LRG_583:g.14811T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.486-13T>C MANE Select	ENSP00000384957.2:n.486-13T>C
ENST00000264692.8:c.324-13T>C	ENSP00000264692.5:n.324-13T>C
ENST00000403665.6:c.486-13T>C	ENSP00000384957.2:n.486-13T>C
NM_000128.3:c.486-13T>C , LRG_583t1:c.486-13T>C	NP_000119.1:n.486-13T>C
XM_005262821.2:c.486-13T>C	XP_005262878.1:n.486-13T>C
XM_005262822.2:c.486-13T>C	XP_005262879.1:n.486-13T>C
XM_005262823.2:c.485+1499T>C	XP_005262880.1:n.485+1499T>C
XM_005262824.1:c.486-13T>C	XP_005262881.1:n.486-13T>C
XM_006714137.1:c.486-13T>C	XP_006714200.1:n.486-13T>C
XR_938706.1:n.838-13T>C
XR_938707.1:n.838-13T>C
XM_005262821.4:c.486-13T>C	XP_005262878.1:n.486-13T>C
XM_005262822.4:c.486-13T>C	XP_005262879.1:n.486-13T>C
XM_005262823.4:c.485+1499T>C	XP_005262880.1:n.485+1499T>C
XM_006714137.3:c.486-13T>C	XP_006714200.1:n.486-13T>C
XM_017007884.2:c.486-13T>C	XP_016863373.1:n.486-13T>C
XM_017007885.2:c.486-13T>C	XP_016863374.1:n.486-13T>C
XM_017007886.2:c.486-13T>C	XP_016863375.1:n.486-13T>C
XR_001741172.2:n.819-13T>C
NM_000128.4:c.486-13T>C MANE Select	NP_000119.1:n.486-13T>C