Canonical Allele Identifier: CA2649657728
Gene: F13B HGNC NCBI

Linked Data

gnomAD v4: 1-197039215-T-TGGTTTTCATTTATA
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039216_197039229dup , CM000663.2:g.197039216_197039229dup GRCh38
NC_000001.10:g.197008346_197008359dup , CM000663.1:g.197008346_197008359dup GRCh37
NC_000001.9:g.195274969_195274982dup NCBI36
NG_012065.1:g.33039_33052dup , LRG_550:g.33039_33052dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*149_*162dup MANE Select ENSP00000356382.2:n.*149_*162dup
ENST00000649282.1:c.890_903dup ENSP00000497116.1:n.890_903dup
ENST00000367412.1:c.*149_*162dup ENSP00000356382.1:n.*149_*162dup
NM_001994.2:c.*149_*162dup , LRG_550t1:c.*149_*162dup NP_001985.2:n.*149_*162dup
XM_011509283.2:c.*1070_*1083dup XP_011507585.1:n.*1070_*1083dup
XM_011509284.2:c.*1070_*1083dup XP_011507586.1:n.*1070_*1083dup
XM_011509286.2:c.*1070_*1083dup XP_011507588.1:n.*1070_*1083dup
NM_001994.3:c.*149_*162dup MANE Select NP_001985.2:n.*149_*162dup
Search 100 bp 5'
Search 100 bp 3'