Canonical Allele Identifier: CA2532805356
Gene: F13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039365del , CM000663.2:g.197039365del GRCh38
NC_000001.10:g.197008495del , CM000663.1:g.197008495del GRCh37
NC_000001.9:g.195275118del NCBI36
NG_012065.1:g.32903del , LRG_550:g.32903del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*13del MANE Select ENSP00000356382.2:n.*13del
ENST00000649282.1:c.754del ENSP00000497116.1:n.754del
ENST00000367412.1:c.*13del ENSP00000356382.1:n.*13del
NM_001994.2:c.*13del , LRG_550t1:c.*13del NP_001985.2:n.*13del
XM_011509283.2:c.*934del XP_011507585.1:n.*934del
XM_011509284.2:c.*934del XP_011507586.1:n.*934del
XM_011509286.2:c.*934del XP_011507588.1:n.*934del
NM_001994.3:c.*13del MANE Select NP_001985.2:n.*13del
Search 100 bp 5'
Search 100 bp 3'