Canonical Allele Identifier: CA1519932339
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186265951A= , CM000666.2:g.186265951A= GRCh38
NC_000004.11:g.187187105A= , CM000666.1:g.187187105A= GRCh37
NC_000004.10:g.187424099A= NCBI36
NG_008051.1:g.4988A= , LRG_583:g.4988A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.6:c.-346A= ENSP00000384957.2:n.-346A=
XM_005262821.2:c.-346A= XP_005262878.1:n.-346A=
XM_005262822.2:c.-346A= XP_005262879.1:n.-346A=
XM_005262823.2:c.-346A= XP_005262880.1:n.-346A=
XM_005262824.1:c.-346A= XP_005262881.1:n.-346A=
XM_006714137.1:c.-346A= XP_006714200.1:n.-346A=
XR_938706.1:n.7A=
XR_938707.1:n.7A=