Canonical Allele Identifier: CA1619211464
Gene: LTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31570486T= , CM000668.2:g.31570486T= GRCh38
NC_000006.11:g.31538263T= , CM000668.1:g.31538263T= GRCh37
NC_000006.10:g.31646242T= NCBI36
NG_012010.1:g.3388T=

Transcript Alleles

HGVS Amino-acid change
XM_011514614.1:c.-341-1006T= XP_011512916.1:n.-341-1006T=
XM_011514615.1:c.-341-1006T= XP_011512917.1:n.-341-1006T=
XM_011514616.1:c.-177-1649T= XP_011512918.1:n.-177-1649T=
XM_011514617.1:c.-341-1006T= XP_011512919.1:n.-341-1006T=
XM_011514618.1:c.-341-1006T= XP_011512920.1:n.-341-1006T=
XR_926695.1:n.116+2097A=
NR_149045.1:n.121+2097A=
XM_011514615.2:c.-341-1006T= XP_011512917.1:n.-341-1006T=
XM_011514616.2:c.-177-1649T= XP_011512918.1:n.-177-1649T=
XM_011514617.2:c.-341-1006T= XP_011512919.1:n.-341-1006T=