Canonical Allele Identifier: CA1619211455
Community Standard Title: NC_000006.12:g.31570467C=
Gene: LTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31570467C= , CM000668.2:g.31570467C= GRCh38
NC_000006.11:g.31538244C= , CM000668.1:g.31538244C= GRCh37
NC_000006.10:g.31646223C= NCBI36
NG_012010.1:g.3369C=

Transcript Alleles

HGVS Amino-acid Change
NR_149045.1:n.121+2116G=
XM_011514614.1:c.-341-1025C= XP_011512916.1:n.-341-1025C=
XM_011514615.1:c.-341-1025C= XP_011512917.1:n.-341-1025C=
XM_011514615.2:c.-341-1025C= XP_011512917.1:n.-341-1025C=
XM_011514616.1:c.-177-1668C= XP_011512918.1:n.-177-1668C=
XM_011514616.2:c.-177-1668C= XP_011512918.1:n.-177-1668C=
XM_011514617.1:c.-341-1025C= XP_011512919.1:n.-341-1025C=
XM_011514617.2:c.-341-1025C= XP_011512919.1:n.-341-1025C=
XM_011514618.1:c.-341-1025C= XP_011512920.1:n.-341-1025C=
XR_926695.1:n.116+2116G=