Canonical Allele Identifier: CA363339309

Gene: LTA

Linked Data

• gnomAD v4: 6-31573025-A-G
• MyVariant Identifiers: chr6:g.31540802A>G (hg19) ; chr6:g.31573025A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31573025A>G , CM000668.2:g.31573025A>G	GRCh38
NC_000006.11:g.31540802A>G , CM000668.1:g.31540802A>G	GRCh37
NC_000006.10:g.31648781A>G	NCBI36
NG_007462.1:g.2453A>G
NG_012010.1:g.5927A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000418386.3:c.197A>G MANE Select	ENSP00000413450.2:p.His66Arg
ENST00000418386.2:c.197A>G	ENSP00000413450.2:p.His66Arg
ENST00000454783.5:c.197A>G	ENSP00000403495.1:p.His66Arg
ENST00000471842.1:n.445A>G
ENST00000489638.5:n.325A>G
NM_000595.3:c.197A>G	NP_000586.2:p.His66Arg
NM_001159740.2:c.197A>G	NP_001153212.1:p.His66Arg
XM_011514614.1:c.197A>G	XP_011512916.1:p.His66Arg
XM_011514615.1:c.197A>G	XP_011512917.1:p.His66Arg
XM_011514616.1:c.197A>G	XP_011512918.1:p.His66Arg
XM_011514617.1:c.197A>G	XP_011512919.1:p.His66Arg
XM_011514618.1:c.197A>G	XP_011512920.1:p.His66Arg
XM_011514615.2:c.197A>G	XP_011512917.1:p.His66Arg
XM_011514616.2:c.197A>G	XP_011512918.1:p.His66Arg
XM_011514617.2:c.197A>G	XP_011512919.1:p.His66Arg
NM_000595.4:c.197A>G MANE Select	NP_000586.2:p.His66Arg