Canonical Allele Identifier: CA1217904226

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039415G= , CM000663.2:g.197039415G=	GRCh38
NC_000001.10:g.197008545G= , CM000663.1:g.197008545G=	GRCh37
NC_000001.9:g.195275168G=	NCBI36
NG_012065.1:g.32853C= , LRG_550:g.32853C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.1953-4C= MANE Select	ENSP00000356382.2:n.1953-4C=
ENST00000649282.1:c.708-4C=	ENSP00000497116.1:n.708-4C=
ENST00000367412.1:c.1953-4C=	ENSP00000356382.1:n.1953-4C=
NM_001994.2:c.1953-4C= , LRG_550t1:c.1953-4C=	NP_001985.2:n.1953-4C=
XM_011509283.2:c.*884C=	XP_011507585.1:n.*884C=
XM_011509284.2:c.*884C=	XP_011507586.1:n.*884C=
XM_011509286.2:c.*884C=	XP_011507588.1:n.*884C=
NM_001994.3:c.1953-4C= MANE Select	NP_001985.2:n.1953-4C=