Canonical Allele Identifier: CA1217904126
Gene: F13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039101A= , CM000663.2:g.197039101A= GRCh38
NC_000001.10:g.197008231A= , CM000663.1:g.197008231A= GRCh37
NC_000001.9:g.195274854A= NCBI36
NG_012065.1:g.33167T= , LRG_550:g.33167T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*277T= MANE Select ENSP00000356382.2:n.*277T=
ENST00000649282.1:c.1018T= ENSP00000497116.1:n.1018T=
XM_011509283.2:c.*1198T= XP_011507585.1:n.*1198T=
XM_011509284.2:c.*1198T= XP_011507586.1:n.*1198T=
XM_011509286.2:c.*1198T= XP_011507588.1:n.*1198T=
NM_001994.3:c.*277T= MANE Select NP_001985.2:n.*277T=
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