Canonical Allele Identifier: CA12368069
Gene: LTA HGNC NCBI
COSMIC:
COSN20351635 (not active)
MyVariant.info:
GRCh38 chr6:g.31570720T>A
GRCh37 chr6:g.31538497T>A
gnomAD v2:
6:31538497 T / A
gnomAD v3:
6:31570720 T / A
gnomAD v4:
chr6-31570720-T-A
Joint Max Group AF 0.55210166 (EAS)
Genomes Max Group AF 0.55210166 (EAS)
dbSNP:
915654
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31570720T>A , CM000668.2:g.31570720T>A GRCh38
NC_000006.11:g.31538497T>A , CM000668.1:g.31538497T>A GRCh37
NC_000006.10:g.31646476T>A NCBI36
NG_007462.1:g.148T>A
NG_012010.1:g.3622T>A

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-341-772T>A XP_011512916.1:n.-341-772T>A
XM_011514615.1:c.-341-772T>A XP_011512917.1:n.-341-772T>A
XM_011514616.1:c.-177-1415T>A XP_011512918.1:n.-177-1415T>A
XM_011514617.1:c.-341-772T>A XP_011512919.1:n.-341-772T>A
XM_011514618.1:c.-341-772T>A XP_011512920.1:n.-341-772T>A
XR_926695.1:n.116+1863A>T
NR_149045.1:n.121+1863A>T
XM_011514615.2:c.-341-772T>A XP_011512917.1:n.-341-772T>A
XM_011514616.2:c.-177-1415T>A XP_011512918.1:n.-177-1415T>A
XM_011514617.2:c.-341-772T>A XP_011512919.1:n.-341-772T>A
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