Canonical Allele Identifier: CA1619211444
Gene: LTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31570441C= , CM000668.2:g.31570441C= GRCh38
NC_000006.11:g.31538218C= , CM000668.1:g.31538218C= GRCh37
NC_000006.10:g.31646197C= NCBI36
NG_012010.1:g.3343C=

Transcript Alleles

HGVS Amino-acid change
XM_011514614.1:c.-341-1051C= XP_011512916.1:n.-341-1051C=
XM_011514615.1:c.-341-1051C= XP_011512917.1:n.-341-1051C=
XM_011514616.1:c.-177-1694C= XP_011512918.1:n.-177-1694C=
XM_011514617.1:c.-341-1051C= XP_011512919.1:n.-341-1051C=
XM_011514618.1:c.-341-1051C= XP_011512920.1:n.-341-1051C=
XR_926695.1:n.116+2142G=
NR_149045.1:n.121+2142G=
XM_011514615.2:c.-341-1051C= XP_011512917.1:n.-341-1051C=
XM_011514616.2:c.-177-1694C= XP_011512918.1:n.-177-1694C=
XM_011514617.2:c.-341-1051C= XP_011512919.1:n.-341-1051C=