Canonical Allele Identifier: CA12231310
Gene: LTA HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.31571991A>G
GRCh37 chr6:g.31539768A>G
gnomAD v2:
6:31539768 A / G
gnomAD v3:
6:31571991 A / G
gnomAD v4:
chr6-31571991-A-G
Joint Max Group AF 0.75359542 (SAS)
Genomes Max Group AF 0.75453265 (SAS)
Exomes Max Group AF 0.57350824 (NFE)
dbSNP:
2071590
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31571991A>G , CM000668.2:g.31571991A>G GRCh38
NC_000006.11:g.31539768A>G , CM000668.1:g.31539768A>G GRCh37
NC_000006.10:g.31647747A>G NCBI36
NG_007462.1:g.1419A>G
NG_012010.1:g.4893A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-177-144A>G XP_011512916.1:n.-177-144A>G
XM_011514615.1:c.-177-144A>G XP_011512917.1:n.-177-144A>G
XM_011514616.1:c.-177-144A>G XP_011512918.1:n.-177-144A>G
XM_011514617.1:c.-177-144A>G XP_011512919.1:n.-177-144A>G
XM_011514618.1:c.-177-144A>G XP_011512920.1:n.-177-144A>G
XR_926695.1:n.116+592T>C
NR_149045.1:n.121+592T>C
XM_011514615.2:c.-177-144A>G XP_011512917.1:n.-177-144A>G
XM_011514616.2:c.-177-144A>G XP_011512918.1:n.-177-144A>G
XM_011514617.2:c.-177-144A>G XP_011512919.1:n.-177-144A>G
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