Canonical Allele Identifier: CA136856028
Gene: LTA HGNC NCBI

Linked Data

dbSNP Id: rs1015863254
gnomAD v2: 6-31531340-G-A
gnomAD v3: 6-31563563-G-A
gnomAD v4: 6-31563563-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31563563G>A , CM000668.2:g.31563563G>A GRCh38
NC_000006.11:g.31531340G>A , CM000668.1:g.31531340G>A GRCh37
NC_000006.10:g.31639319G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-342+2294G>A XP_011512916.1:n.-342+2294G>A
XM_011514615.1:c.-342+1096G>A XP_011512917.1:n.-342+1096G>A
XM_011514616.1:c.-178+2294G>A XP_011512918.1:n.-178+2294G>A
XM_011514617.1:c.-342+2294G>A XP_011512919.1:n.-342+2294G>A
XM_011514618.1:c.-342+2294G>A XP_011512920.1:n.-342+2294G>A
XR_926695.1:n.116+9020C>T
NR_149045.1:n.122-2841C>T
XM_011514615.2:c.-342+1096G>A XP_011512917.1:n.-342+1096G>A
XM_011514616.2:c.-178+2294G>A XP_011512918.1:n.-178+2294G>A
XM_011514617.2:c.-342+2294G>A XP_011512919.1:n.-342+2294G>A