Canonical Allele Identifier: CA1619208769
Gene: LTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31563594G= , CM000668.2:g.31563594G= GRCh38
NC_000006.11:g.31531371G= , CM000668.1:g.31531371G= GRCh37
NC_000006.10:g.31639350G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-342+2325G= XP_011512916.1:n.-342+2325G=
XM_011514615.1:c.-342+1127G= XP_011512917.1:n.-342+1127G=
XM_011514616.1:c.-178+2325G= XP_011512918.1:n.-178+2325G=
XM_011514617.1:c.-342+2325G= XP_011512919.1:n.-342+2325G=
XM_011514618.1:c.-342+2325G= XP_011512920.1:n.-342+2325G=
XR_926695.1:n.116+8989C=
NR_149045.1:n.122-2872C=
XM_011514615.2:c.-342+1127G= XP_011512917.1:n.-342+1127G=
XM_011514616.2:c.-178+2325G= XP_011512918.1:n.-178+2325G=
XM_011514617.2:c.-342+2325G= XP_011512919.1:n.-342+2325G=