Canonical Allele Identifier: CA792348311
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1455034546
gnomAD v3: 4-186265949-G-A
gnomAD v4: 4-186265949-G-A
MyVariant Identifiers: chr4:g.187187103G>A (hg19) chr4:g.186265949G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186265949G>A , CM000666.2:g.186265949G>A GRCh38
NC_000004.11:g.187187103G>A , CM000666.1:g.187187103G>A GRCh37
NC_000004.10:g.187424097G>A NCBI36
NG_008051.1:g.4986G>A , LRG_583:g.4986G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.6:c.-348G>A ENSP00000384957.2:n.-348G>A
XM_005262821.2:c.-348G>A XP_005262878.1:n.-348G>A
XM_005262822.2:c.-348G>A XP_005262879.1:n.-348G>A
XM_005262823.2:c.-348G>A XP_005262880.1:n.-348G>A
XM_005262824.1:c.-348G>A XP_005262881.1:n.-348G>A
XM_006714137.1:c.-348G>A XP_006714200.1:n.-348G>A
XR_938706.1:n.5G>A
XR_938707.1:n.5G>A
Search 100 bp 5'
Search 100 bp 3'