Canonical Allele Identifier: CA2649657753
Gene: F13B HGNC NCBI

Linked Data

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

HGVS Genome Assembly
NC_000001.11:g.197039233_197039235del , CM000663.2:g.197039233_197039235del GRCh38
NC_000001.10:g.197008363_197008365del , CM000663.1:g.197008363_197008365del GRCh37
NC_000001.9:g.195274986_195274988del NCBI36
NG_012065.1:g.33033_33035del , LRG_550:g.33033_33035del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*143_*145del MANE Select ENSP00000356382.2:n.*143_*145del
ENST00000649282.1:c.884_886del ENSP00000497116.1:n.884_886del
ENST00000367412.1:c.*143_*145del ENSP00000356382.1:n.*143_*145del
NM_001994.2:c.*143_*145del , LRG_550t1:c.*143_*145del NP_001985.2:n.*143_*145del
XM_011509283.2:c.*1064_*1066del XP_011507585.1:n.*1064_*1066del
XM_011509284.2:c.*1064_*1066del XP_011507586.1:n.*1064_*1066del
XM_011509286.2:c.*1064_*1066del XP_011507588.1:n.*1064_*1066del
NM_001994.3:c.*143_*145del MANE Select NP_001985.2:n.*143_*145del
Search 100 bp 5'
Search 100 bp 3'