Canonical Allele Identifier: CA1146435152
Gene: F13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039170T= , CM000663.2:g.197039170T= GRCh38
NC_000001.10:g.197008300T= , CM000663.1:g.197008300T= GRCh37
NC_000001.9:g.195274923T= NCBI36
NG_012065.1:g.33098A= , LRG_550:g.33098A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*208A= MANE Select ENSP00000356382.2:n.*208A=
ENST00000649282.1:c.949A= ENSP00000497116.1:n.949A=
XM_011509283.2:c.*1129A= XP_011507585.1:n.*1129A=
XM_011509284.2:c.*1129A= XP_011507586.1:n.*1129A=
XM_011509286.2:c.*1129A= XP_011507588.1:n.*1129A=
NM_001994.3:c.*208A= MANE Select NP_001985.2:n.*208A=
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