Canonical Allele Identifier: CA1217904199

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039336C= , CM000663.2:g.197039336C=	GRCh38
NC_000001.10:g.197008466C= , CM000663.1:g.197008466C=	GRCh37
NC_000001.9:g.195275089C=	NCBI36
NG_012065.1:g.32932G= , LRG_550:g.32932G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.*42G= MANE Select	ENSP00000356382.2:n.*42G=
ENST00000649282.1:c.783G=	ENSP00000497116.1:n.783G=
ENST00000367412.1:c.*42G=	ENSP00000356382.1:n.*42G=
NM_001994.2:c.*42G= , LRG_550t1:c.*42G=	NP_001985.2:n.*42G=
XM_011509283.2:c.*963G=	XP_011507585.1:n.*963G=
XM_011509284.2:c.*963G=	XP_011507586.1:n.*963G=
XM_011509286.2:c.*963G=	XP_011507588.1:n.*963G=
NM_001994.3:c.*42G= MANE Select	NP_001985.2:n.*42G=