Canonical Allele Identifier: CA1217911203

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197055724C= , CM000663.2:g.197055724C=	GRCh38
NC_000001.10:g.197024854C= , CM000663.1:g.197024854C=	GRCh37
NC_000001.9:g.195291477C=	NCBI36
NG_012065.1:g.16544G= , LRG_550:g.16544G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.1345G= MANE Select	ENSP00000356382.2:p.Val449=
ENST00000649282.1:c.100G=	ENSP00000497116.1:p.Val34=
ENST00000367412.1:c.1345G=	ENSP00000356382.1:p.Val449=
NM_001994.2:c.1345G= , LRG_550t1:c.1345G=	NP_001985.2:p.Val449=
XM_011509283.1:c.1345G=	XP_011507585.1:p.Val449=
XM_011509284.1:c.1342G=	XP_011507586.1:p.Val448=
XM_011509285.1:c.1249G=	XP_011507587.1:p.Val417=
XM_011509286.1:c.1201G=	XP_011507588.1:p.Val401=
XM_011509283.2:c.1345G=	XP_011507585.1:p.Val449=
XM_011509284.2:c.1342G=	XP_011507586.1:p.Val448=
XM_011509286.2:c.1201G=	XP_011507588.1:p.Val401=
NM_001994.3:c.1345G= MANE Select	NP_001985.2:p.Val449=