Canonical Allele Identifier: CA112146200

Gene: F11

Linked Data

• dbSNP Id: rs569224372
• gnomAD v4: 4-186265963-C-T
• MyVariant Identifiers: chr4:g.187187117C>T (hg19) ; chr4:g.186265963C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186265963C>T , CM000666.2:g.186265963C>T	GRCh38
NC_000004.11:g.187187117C>T , CM000666.1:g.187187117C>T	GRCh37
NC_000004.10:g.187424111C>T	NCBI36
NG_008051.1:g.5000C>T , LRG_583:g.5000C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.6:c.-334C>T	ENSP00000384957.2:n.-334C>T
XM_005262821.2:c.-334C>T	XP_005262878.1:n.-334C>T
XM_005262822.2:c.-334C>T	XP_005262879.1:n.-334C>T
XM_005262823.2:c.-334C>T	XP_005262880.1:n.-334C>T
XM_005262824.1:c.-334C>T	XP_005262881.1:n.-334C>T
XM_006714137.1:c.-334C>T	XP_006714200.1:n.-334C>T
XR_938706.1:n.19C>T
XR_938707.1:n.19C>T