Canonical Allele Identifier: CA1619208698
Gene: LTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31563488A= , CM000668.2:g.31563488A= GRCh38
NC_000006.11:g.31531265A= , CM000668.1:g.31531265A= GRCh37
NC_000006.10:g.31639244A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011514614.1:c.-342+2219A= XP_011512916.1:n.-342+2219A=
XM_011514615.1:c.-342+1021A= XP_011512917.1:n.-342+1021A=
XM_011514616.1:c.-178+2219A= XP_011512918.1:n.-178+2219A=
XM_011514617.1:c.-342+2219A= XP_011512919.1:n.-342+2219A=
XM_011514618.1:c.-342+2219A= XP_011512920.1:n.-342+2219A=
XR_926695.1:n.116+9095T=
NR_149045.1:n.122-2766T=
XM_011514615.2:c.-342+1021A= XP_011512917.1:n.-342+1021A=
XM_011514616.2:c.-178+2219A= XP_011512918.1:n.-178+2219A=
XM_011514617.2:c.-342+2219A= XP_011512919.1:n.-342+2219A=