Canonical Allele Identifier: CA823885427
Gene: LTA HGNC NCBI

Linked Data

dbSNP Id: rs1386325173
gnomAD v3: 6-31563537-A-G
gnomAD v4: 6-31563537-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31563537A>G , CM000668.2:g.31563537A>G GRCh38
NC_000006.11:g.31531314A>G , CM000668.1:g.31531314A>G GRCh37
NC_000006.10:g.31639293A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-342+2268A>G XP_011512916.1:n.-342+2268A>G
XM_011514615.1:c.-342+1070A>G XP_011512917.1:n.-342+1070A>G
XM_011514616.1:c.-178+2268A>G XP_011512918.1:n.-178+2268A>G
XM_011514617.1:c.-342+2268A>G XP_011512919.1:n.-342+2268A>G
XM_011514618.1:c.-342+2268A>G XP_011512920.1:n.-342+2268A>G
XR_926695.1:n.116+9046T>C
NR_149045.1:n.122-2815T>C
XM_011514615.2:c.-342+1070A>G XP_011512917.1:n.-342+1070A>G
XM_011514616.2:c.-178+2268A>G XP_011512918.1:n.-178+2268A>G
XM_011514617.2:c.-342+2268A>G XP_011512919.1:n.-342+2268A>G