Canonical Allele Identifier: CA2698077118
Gene: F13B HGNC NCBI

Linked Data

dbSNP Id: rs2125050709
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039149A>T , CM000663.2:g.197039149A>T GRCh38
NC_000001.10:g.197008279A>T , CM000663.1:g.197008279A>T GRCh37
NC_000001.9:g.195274902A>T NCBI36
NG_012065.1:g.33119T>A , LRG_550:g.33119T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*229T>A MANE Select ENSP00000356382.2:n.*229T>A
ENST00000649282.1:c.970T>A ENSP00000497116.1:n.970T>A
XM_011509283.2:c.*1150T>A XP_011507585.1:n.*1150T>A
XM_011509284.2:c.*1150T>A XP_011507586.1:n.*1150T>A
XM_011509286.2:c.*1150T>A XP_011507588.1:n.*1150T>A
NM_001994.3:c.*229T>A MANE Select NP_001985.2:n.*229T>A
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