Canonical Allele Identifier: CA2056511079

Gene: LTA4H

Linked Data

• dbSNP Id: rs1950649106

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.96036552A>C , CM000674.2:g.96036552A>C	GRCh38
NC_000012.11:g.96430330A>C , CM000674.1:g.96430330A>C	GRCh37
NC_000012.10:g.94954461A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000413268.6:c.87+6737T>G	ENSP00000395051.2:n.87+6737T>G
ENST00000552789.5:c.87+6737T>G	ENSP00000449958.1:n.87+6737T>G
NM_001256643.1:c.87+6737T>G	NP_001243572.1:n.87+6737T>G
NM_001256644.1:c.87+6737T>G	NP_001243573.1:n.87+6737T>G