Canonical Allele Identifier: CA2573973402
Gene: F13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039319T>A , CM000663.2:g.197039319T>A GRCh38
NC_000001.10:g.197008449T>A , CM000663.1:g.197008449T>A GRCh37
NC_000001.9:g.195275072T>A NCBI36
NG_012065.1:g.32949A>T , LRG_550:g.32949A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367412.2:c.*59A>T MANE Select ENSP00000356382.2:n.*59A>T
ENST00000649282.1:c.800A>T ENSP00000497116.1:n.800A>T
ENST00000367412.1:c.*59A>T ENSP00000356382.1:n.*59A>T
NM_001994.2:c.*59A>T , LRG_550t1:c.*59A>T NP_001985.2:n.*59A>T
XM_011509283.2:c.*980A>T XP_011507585.1:n.*980A>T
XM_011509284.2:c.*980A>T XP_011507586.1:n.*980A>T
XM_011509286.2:c.*980A>T XP_011507588.1:n.*980A>T
NM_001994.3:c.*59A>T MANE Select NP_001985.2:n.*59A>T