Canonical Allele Identifier: CA1147887830
Gene: F13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039185A= , CM000663.2:g.197039185A= GRCh38
NC_000001.10:g.197008315A= , CM000663.1:g.197008315A= GRCh37
NC_000001.9:g.195274938A= NCBI36
NG_012065.1:g.33083T= , LRG_550:g.33083T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*193T= MANE Select ENSP00000356382.2:n.*193T=
ENST00000649282.1:c.934T= ENSP00000497116.1:n.934T=
XM_011509283.2:c.*1114T= XP_011507585.1:n.*1114T=
XM_011509284.2:c.*1114T= XP_011507586.1:n.*1114T=
XM_011509286.2:c.*1114T= XP_011507588.1:n.*1114T=
NM_001994.3:c.*193T= MANE Select NP_001985.2:n.*193T=
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