Canonical Allele Identifier: CA1217904141
Gene: F13B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039158A= , CM000663.2:g.197039158A= GRCh38
NC_000001.10:g.197008288A= , CM000663.1:g.197008288A= GRCh37
NC_000001.9:g.195274911A= NCBI36
NG_012065.1:g.33110T= , LRG_550:g.33110T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*220T= MANE Select ENSP00000356382.2:n.*220T=
ENST00000649282.1:c.961T= ENSP00000497116.1:n.961T=
XM_011509283.2:c.*1141T= XP_011507585.1:n.*1141T=
XM_011509284.2:c.*1141T= XP_011507586.1:n.*1141T=
XM_011509286.2:c.*1141T= XP_011507588.1:n.*1141T=
NM_001994.3:c.*220T= MANE Select NP_001985.2:n.*220T=
Search 100 bp 5'
Search 100 bp 3'