Canonical Allele Identifier: CA2056511102
Gene: LTA4H HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.96036598G= , CM000674.2:g.96036598G= GRCh38
NC_000012.11:g.96430376G= , CM000674.1:g.96430376G= GRCh37
NC_000012.10:g.94954507G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000413268.6:c.87+6691C= ENSP00000395051.2:n.87+6691C=
ENST00000552789.5:c.87+6691C= ENSP00000449958.1:n.87+6691C=
NM_001256643.1:c.87+6691C= NP_001243572.1:n.87+6691C=
NM_001256644.1:c.87+6691C= NP_001243573.1:n.87+6691C=
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