Canonical Allele Identifier: CA1217904125
Gene: F13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039099C= , CM000663.2:g.197039099C= GRCh38
NC_000001.10:g.197008229C= , CM000663.1:g.197008229C= GRCh37
NC_000001.9:g.195274852C= NCBI36
NG_012065.1:g.33169G= , LRG_550:g.33169G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*279G= MANE Select ENSP00000356382.2:n.*279G=
ENST00000649282.1:c.1020G= ENSP00000497116.1:n.1020G=
XM_011509283.2:c.*1200G= XP_011507585.1:n.*1200G=
XM_011509284.2:c.*1200G= XP_011507586.1:n.*1200G=
XM_011509286.2:c.*1200G= XP_011507588.1:n.*1200G=
NM_001994.3:c.*279G= MANE Select NP_001985.2:n.*279G=
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