Canonical Allele Identifier: CA693786852
Gene: LTA4H HGNC NCBI

Linked Data

dbSNP Id: rs1169267305
gnomAD v3: 12-96036581-C-T
gnomAD v4: 12-96036581-C-T
MyVariant Identifiers: chr12:g.96430359C>T (hg19) chr12:g.96036581C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.96036581C>T , CM000674.2:g.96036581C>T GRCh38
NC_000012.11:g.96430359C>T , CM000674.1:g.96430359C>T GRCh37
NC_000012.10:g.94954490C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000413268.6:c.87+6708G>A ENSP00000395051.2:n.87+6708G>A
ENST00000552789.5:c.87+6708G>A ENSP00000449958.1:n.87+6708G>A
NM_001256643.1:c.87+6708G>A NP_001243572.1:n.87+6708G>A
NM_001256644.1:c.87+6708G>A NP_001243573.1:n.87+6708G>A
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