Canonical Allele Identifier: CA1217904144
Gene: F13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039161C= , CM000663.2:g.197039161C= GRCh38
NC_000001.10:g.197008291C= , CM000663.1:g.197008291C= GRCh37
NC_000001.9:g.195274914C= NCBI36
NG_012065.1:g.33107G= , LRG_550:g.33107G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*217G= MANE Select ENSP00000356382.2:n.*217G=
ENST00000649282.1:c.958G= ENSP00000497116.1:n.958G=
XM_011509283.2:c.*1138G= XP_011507585.1:n.*1138G=
XM_011509284.2:c.*1138G= XP_011507586.1:n.*1138G=
XM_011509286.2:c.*1138G= XP_011507588.1:n.*1138G=
NM_001994.3:c.*217G= MANE Select NP_001985.2:n.*217G=