Canonical Allele Identifier: CA2747238368
Gene: F13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039182T>G , CM000663.2:g.197039182T>G GRCh38
NC_000001.10:g.197008312T>G , CM000663.1:g.197008312T>G GRCh37
NC_000001.9:g.195274935T>G NCBI36
NG_012065.1:g.33086A>C , LRG_550:g.33086A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*196A>C MANE Select ENSP00000356382.2:n.*196A>C
ENST00000649282.1:c.937A>C ENSP00000497116.1:n.937A>C
XM_011509283.2:c.*1117A>C XP_011507585.1:n.*1117A>C
XM_011509284.2:c.*1117A>C XP_011507586.1:n.*1117A>C
XM_011509286.2:c.*1117A>C XP_011507588.1:n.*1117A>C
NM_001994.3:c.*196A>C MANE Select NP_001985.2:n.*196A>C
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