Canonical Allele Identifier: CA12266079
Gene: LTA HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.31571990C>T
GRCh37 chr6:g.31539767C>T
gnomAD v2:
6:31539767 C / T
gnomAD v3:
6:31571990 C / T
gnomAD v4:
chr6-31571990-C-T
Joint Max Group AF 0.23539712 (SAS)
Genomes Max Group AF 0.23592014 (SAS)
Exomes Max Group AF 0.09781709 (SAS)
dbSNP:
2844482
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31571990C>T , CM000668.2:g.31571990C>T GRCh38
NC_000006.11:g.31539767C>T , CM000668.1:g.31539767C>T GRCh37
NC_000006.10:g.31647746C>T NCBI36
NG_007462.1:g.1418C>T
NG_012010.1:g.4892C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-177-145C>T XP_011512916.1:n.-177-145C>T
XM_011514615.1:c.-177-145C>T XP_011512917.1:n.-177-145C>T
XM_011514616.1:c.-177-145C>T XP_011512918.1:n.-177-145C>T
XM_011514617.1:c.-177-145C>T XP_011512919.1:n.-177-145C>T
XM_011514618.1:c.-177-145C>T XP_011512920.1:n.-177-145C>T
XR_926695.1:n.116+593G>A
NR_149045.1:n.121+593G>A
XM_011514615.2:c.-177-145C>T XP_011512917.1:n.-177-145C>T
XM_011514616.2:c.-177-145C>T XP_011512918.1:n.-177-145C>T
XM_011514617.2:c.-177-145C>T XP_011512919.1:n.-177-145C>T
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