Canonical Allele Identifier: CA1217904114

Gene: F13B

Linked Data

• dbSNP Id: rs1654943631

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039088_197039098del , CM000663.2:g.197039088_197039098del	GRCh38
NC_000001.10:g.197008218_197008228del , CM000663.1:g.197008218_197008228del	GRCh37
NC_000001.9:g.195274841_195274851del	NCBI36
NG_012065.1:g.33170_33180del , LRG_550:g.33170_33180del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*280_*290del MANE Select	ENSP00000356382.2:n.*280_*290del
ENST00000649282.1:c.1021_1031del	ENSP00000497116.1:n.1021_1031del
XM_011509283.2:c.*1201_*1211del	XP_011507585.1:n.*1201_*1211del
XM_011509284.2:c.*1201_*1211del	XP_011507586.1:n.*1201_*1211del
XM_011509286.2:c.*1201_*1211del	XP_011507588.1:n.*1201_*1211del
NM_001994.3:c.*280_*290del MANE Select	NP_001985.2:n.*280_*290del