Canonical Allele Identifier: CA2649657754
Gene: F13B HGNC NCBI

Linked Data

gnomAD v4: 1-197039232-T-TGAA
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039232_197039233insGAA , CM000663.2:g.197039232_197039233insGAA GRCh38
NC_000001.10:g.197008362_197008363insGAA , CM000663.1:g.197008362_197008363insGAA GRCh37
NC_000001.9:g.195274985_195274986insGAA NCBI36
NG_012065.1:g.33035_33036insTTC , LRG_550:g.33035_33036insTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*145_*146insTTC MANE Select ENSP00000356382.2:n.*145_*146insTTC
ENST00000649282.1:c.886_887insTTC ENSP00000497116.1:n.886_887insTTC
ENST00000367412.1:c.*145_*146insTTC ENSP00000356382.1:n.*145_*146insTTC
NM_001994.2:c.*145_*146insTTC , LRG_550t1:c.*145_*146insTTC NP_001985.2:n.*145_*146insTTC
XM_011509283.2:c.*1066_*1067insTTC XP_011507585.1:n.*1066_*1067insTTC
XM_011509284.2:c.*1066_*1067insTTC XP_011507586.1:n.*1066_*1067insTTC
XM_011509286.2:c.*1066_*1067insTTC XP_011507588.1:n.*1066_*1067insTTC
NM_001994.3:c.*145_*146insTTC MANE Select NP_001985.2:n.*145_*146insTTC
Search 100 bp 5'
Search 100 bp 3'