Canonical Allele Identifier: CA1217904249

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039457T= , CM000663.2:g.197039457T=	GRCh38
NC_000001.10:g.197008587T= , CM000663.1:g.197008587T=	GRCh37
NC_000001.9:g.195275210T=	NCBI36
NG_012065.1:g.32811A= , LRG_550:g.32811A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.1953-46A= MANE Select	ENSP00000356382.2:n.1953-46A=
ENST00000649282.1:c.708-46A=	ENSP00000497116.1:n.708-46A=
ENST00000367412.1:c.1953-46A=	ENSP00000356382.1:n.1953-46A=
NM_001994.2:c.1953-46A= , LRG_550t1:c.1953-46A=	NP_001985.2:n.1953-46A=
XM_011509283.2:c.*842A=	XP_011507585.1:n.*842A=
XM_011509284.2:c.*842A=	XP_011507586.1:n.*842A=
XM_011509286.2:c.*842A=	XP_011507588.1:n.*842A=
NM_001994.3:c.1953-46A= MANE Select	NP_001985.2:n.1953-46A=