Canonical Allele Identifier: CA1217904142
Gene: F13B HGNC NCBI

Linked Data

dbSNP Id: rs1654946281
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Genomic Alleles

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

Transcript Alleles

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