Canonical Allele Identifier: CA2672900956
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186265966G>T , CM000666.2:g.186265966G>T GRCh38
NC_000004.11:g.187187120G>T , CM000666.1:g.187187120G>T GRCh37
NC_000004.10:g.187424114G>T NCBI36
NG_008051.1:g.5003G>T , LRG_583:g.5003G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.6:c.-331G>T ENSP00000384957.2:n.-331G>T
NM_000128.3:c.-331G>T , LRG_583t1:c.-331G>T NP_000119.1:n.-331G>T
XM_005262821.2:c.-331G>T XP_005262878.1:n.-331G>T
XM_005262822.2:c.-331G>T XP_005262879.1:n.-331G>T
XM_005262823.2:c.-331G>T XP_005262880.1:n.-331G>T
XM_005262824.1:c.-331G>T XP_005262881.1:n.-331G>T
XM_006714137.1:c.-331G>T XP_006714200.1:n.-331G>T
XR_938706.1:n.22G>T
XR_938707.1:n.22G>T
NM_001354804.1:c.-331G>T NP_001341733.1:n.-331G>T
XM_005262821.4:c.-331G>T XP_005262878.1:n.-331G>T
XM_005262822.4:c.-331G>T XP_005262879.1:n.-331G>T
XM_005262823.4:c.-331G>T XP_005262880.1:n.-331G>T
XM_006714137.3:c.-331G>T XP_006714200.1:n.-331G>T
XM_017007884.2:c.-331G>T XP_016863373.1:n.-331G>T
XM_017007885.2:c.-331G>T XP_016863374.1:n.-331G>T
XM_017007886.2:c.-331G>T XP_016863375.1:n.-331G>T
XR_001741172.2:n.3G>T