Canonical Allele Identifier: CA2564678839
Gene: F13B HGNC NCBI

Linked Data

gnomAD v4: 1-197039145-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039146del , CM000663.2:g.197039146del GRCh38
NC_000001.10:g.197008276del , CM000663.1:g.197008276del GRCh37
NC_000001.9:g.195274899del NCBI36
NG_012065.1:g.33122del , LRG_550:g.33122del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*232del MANE Select ENSP00000356382.2:n.*232del
ENST00000649282.1:c.973del ENSP00000497116.1:n.973del
XM_011509283.2:c.*1153del XP_011507585.1:n.*1153del
XM_011509284.2:c.*1153del XP_011507586.1:n.*1153del
XM_011509286.2:c.*1153del XP_011507588.1:n.*1153del
NM_001994.3:c.*232del MANE Select NP_001985.2:n.*232del
Search 100 bp 5'
Search 100 bp 3'