Canonical Allele Identifier: CA2649657847
Gene: F13B HGNC NCBI

Linked Data

gnomAD v4: 1-197039357-TC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039359del , CM000663.2:g.197039359del GRCh38
NC_000001.10:g.197008489del , CM000663.1:g.197008489del GRCh37
NC_000001.9:g.195275112del NCBI36
NG_012065.1:g.32910del , LRG_550:g.32910del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*20del MANE Select ENSP00000356382.2:n.*20del
ENST00000649282.1:c.761del ENSP00000497116.1:n.761del
ENST00000367412.1:c.*20del ENSP00000356382.1:n.*20del
NM_001994.2:c.*20del , LRG_550t1:c.*20del NP_001985.2:n.*20del
XM_011509283.2:c.*941del XP_011507585.1:n.*941del
XM_011509284.2:c.*941del XP_011507586.1:n.*941del
XM_011509286.2:c.*941del XP_011507588.1:n.*941del
NM_001994.3:c.*20del MANE Select NP_001985.2:n.*20del
Search 100 bp 5'
Search 100 bp 3'