Canonical Allele Identifier: CA1619208742
Gene: LTA HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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