Canonical Allele Identifier: CA1519932342
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186265959C= , CM000666.2:g.186265959C= GRCh38
NC_000004.11:g.187187113C= , CM000666.1:g.187187113C= GRCh37
NC_000004.10:g.187424107C= NCBI36
NG_008051.1:g.4996C= , LRG_583:g.4996C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.6:c.-338C= ENSP00000384957.2:n.-338C=
XM_005262821.2:c.-338C= XP_005262878.1:n.-338C=
XM_005262822.2:c.-338C= XP_005262879.1:n.-338C=
XM_005262823.2:c.-338C= XP_005262880.1:n.-338C=
XM_005262824.1:c.-338C= XP_005262881.1:n.-338C=
XM_006714137.1:c.-338C= XP_006714200.1:n.-338C=
XR_938706.1:n.15C=
XR_938707.1:n.15C=