Canonical Allele Identifier: CA1217904151
Gene: F13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039174G= , CM000663.2:g.197039174G= GRCh38
NC_000001.10:g.197008304G= , CM000663.1:g.197008304G= GRCh37
NC_000001.9:g.195274927G= NCBI36
NG_012065.1:g.33094C= , LRG_550:g.33094C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*204C= MANE Select ENSP00000356382.2:n.*204C=
ENST00000649282.1:c.945C= ENSP00000497116.1:n.945C=
XM_011509283.2:c.*1125C= XP_011507585.1:n.*1125C=
XM_011509284.2:c.*1125C= XP_011507586.1:n.*1125C=
XM_011509286.2:c.*1125C= XP_011507588.1:n.*1125C=
NM_001994.3:c.*204C= MANE Select NP_001985.2:n.*204C=
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