Canonical Allele Identifier: CA1217911655

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197056950G= , CM000663.2:g.197056950G=	GRCh38
NC_000001.10:g.197026080G= , CM000663.1:g.197026080G=	GRCh37
NC_000001.9:g.195292703G=	NCBI36
NG_012065.1:g.15318C= , LRG_550:g.15318C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.1171+63C= MANE Select	ENSP00000356382.2:n.1171+63C=
ENST00000367412.1:c.1171+63C=	ENSP00000356382.1:n.1171+63C=
NM_001994.2:c.1171+63C= , LRG_550t1:c.1171+63C=	NP_001985.2:n.1171+63C=
XM_011509283.1:c.1171+63C=	XP_011507585.1:n.1171+63C=
XM_011509284.1:c.1168+63C=	XP_011507586.1:n.1168+63C=
XM_011509285.1:c.1075+63C=	XP_011507587.1:n.1075+63C=
XM_011509286.1:c.1027+63C=	XP_011507588.1:n.1027+63C=
XM_011509283.2:c.1171+63C=	XP_011507585.1:n.1171+63C=
XM_011509284.2:c.1168+63C=	XP_011507586.1:n.1168+63C=
XM_011509286.2:c.1027+63C=	XP_011507588.1:n.1027+63C=
NM_001994.3:c.1171+63C= MANE Select	NP_001985.2:n.1171+63C=