Canonical Allele Identifier: CA2537569539
Gene: F13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039155_197039161del , CM000663.2:g.197039155_197039161del GRCh38
NC_000001.10:g.197008285_197008291del , CM000663.1:g.197008285_197008291del GRCh37
NC_000001.9:g.195274908_195274914del NCBI36
NG_012065.1:g.33107_33113del , LRG_550:g.33107_33113del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*217_*223del MANE Select ENSP00000356382.2:n.*217_*223del
ENST00000649282.1:c.958_964del ENSP00000497116.1:n.958_964del
XM_011509283.2:c.*1138_*1144del XP_011507585.1:n.*1138_*1144del
XM_011509284.2:c.*1138_*1144del XP_011507586.1:n.*1138_*1144del
XM_011509286.2:c.*1138_*1144del XP_011507588.1:n.*1138_*1144del
NM_001994.3:c.*217_*223del MANE Select NP_001985.2:n.*217_*223del