Canonical Allele Identifier: CA645846982

Gene: F13B

Linked Data

• COSMIC: COSN22294267

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039155G>A , CM000663.2:g.197039155G>A	GRCh38
NC_000001.10:g.197008285G>A , CM000663.1:g.197008285G>A	GRCh37
NC_000001.9:g.195274908G>A	NCBI36
NG_012065.1:g.33113C>T , LRG_550:g.33113C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*223C>T MANE Select	ENSP00000356382.2:n.*223C>T
ENST00000649282.1:c.964C>T	ENSP00000497116.1:n.964C>T
XM_011509283.2:c.*1144C>T	XP_011507585.1:n.*1144C>T
XM_011509284.2:c.*1144C>T	XP_011507586.1:n.*1144C>T
XM_011509286.2:c.*1144C>T	XP_011507588.1:n.*1144C>T
NM_001994.3:c.*223C>T MANE Select	NP_001985.2:n.*223C>T