Canonical Allele Identifier: CA2649657697
Gene: F13B HGNC NCBI

Linked Data

gnomAD v4: 1-197039170-T-TG
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039170_197039171insG , CM000663.2:g.197039170_197039171insG GRCh38
NC_000001.10:g.197008300_197008301insG , CM000663.1:g.197008300_197008301insG GRCh37
NC_000001.9:g.195274923_195274924insG NCBI36
NG_012065.1:g.33097_33098insC , LRG_550:g.33097_33098insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*207_*208insC MANE Select ENSP00000356382.2:n.*207_*208insC
ENST00000649282.1:c.948_949insC ENSP00000497116.1:n.948_949insC
XM_011509283.2:c.*1128_*1129insC XP_011507585.1:n.*1128_*1129insC
XM_011509284.2:c.*1128_*1129insC XP_011507586.1:n.*1128_*1129insC
XM_011509286.2:c.*1128_*1129insC XP_011507588.1:n.*1128_*1129insC
NM_001994.3:c.*207_*208insC MANE Select NP_001985.2:n.*207_*208insC
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