Canonical Allele Identifier: CA1217904127
Gene: F13B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039108T= , CM000663.2:g.197039108T= GRCh38
NC_000001.10:g.197008238T= , CM000663.1:g.197008238T= GRCh37
NC_000001.9:g.195274861T= NCBI36
NG_012065.1:g.33160A= , LRG_550:g.33160A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*270A= MANE Select ENSP00000356382.2:n.*270A=
ENST00000649282.1:c.1011A= ENSP00000497116.1:n.1011A=
XM_011509283.2:c.*1191A= XP_011507585.1:n.*1191A=
XM_011509284.2:c.*1191A= XP_011507586.1:n.*1191A=
XM_011509286.2:c.*1191A= XP_011507588.1:n.*1191A=
NM_001994.3:c.*270A= MANE Select NP_001985.2:n.*270A=
Search 100 bp 5'
Search 100 bp 3'