Canonical Allele Identifier: CA2573973322
Gene: F13B HGNC NCBI

Linked Data

gnomAD v4: 1-197039289-CG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039290del , CM000663.2:g.197039290del GRCh38
NC_000001.10:g.197008420del , CM000663.1:g.197008420del GRCh37
NC_000001.9:g.195275043del NCBI36
NG_012065.1:g.32978del , LRG_550:g.32978del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*88del MANE Select ENSP00000356382.2:n.*88del
ENST00000649282.1:c.829del ENSP00000497116.1:n.829del
ENST00000367412.1:c.*88del ENSP00000356382.1:n.*88del
NM_001994.2:c.*88del , LRG_550t1:c.*88del NP_001985.2:n.*88del
XM_011509283.2:c.*1009del XP_011507585.1:n.*1009del
XM_011509284.2:c.*1009del XP_011507586.1:n.*1009del
XM_011509286.2:c.*1009del XP_011507588.1:n.*1009del
NM_001994.3:c.*88del MANE Select NP_001985.2:n.*88del
Search 100 bp 5'
Search 100 bp 3'