Canonical Allele Identifier: CA1619208732
Gene: LTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31563534C= , CM000668.2:g.31563534C= GRCh38
NC_000006.11:g.31531311C= , CM000668.1:g.31531311C= GRCh37
NC_000006.10:g.31639290C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-342+2265C= XP_011512916.1:n.-342+2265C=
XM_011514615.1:c.-342+1067C= XP_011512917.1:n.-342+1067C=
XM_011514616.1:c.-178+2265C= XP_011512918.1:n.-178+2265C=
XM_011514617.1:c.-342+2265C= XP_011512919.1:n.-342+2265C=
XM_011514618.1:c.-342+2265C= XP_011512920.1:n.-342+2265C=
XR_926695.1:n.116+9049G=
NR_149045.1:n.122-2812G=
XM_011514615.2:c.-342+1067C= XP_011512917.1:n.-342+1067C=
XM_011514616.2:c.-178+2265C= XP_011512918.1:n.-178+2265C=
XM_011514617.2:c.-342+2265C= XP_011512919.1:n.-342+2265C=