Canonical Allele Identifier: CA1619208688

Gene: LTA

Linked Data

• dbSNP Id: rs1770282632

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31563467G>A , CM000668.2:g.31563467G>A	GRCh38
NC_000006.11:g.31531244G>A , CM000668.1:g.31531244G>A	GRCh37
NC_000006.10:g.31639223G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011514614.1:c.-342+2198G>A	XP_011512916.1:n.-342+2198G>A
XM_011514615.1:c.-342+1000G>A	XP_011512917.1:n.-342+1000G>A
XM_011514616.1:c.-178+2198G>A	XP_011512918.1:n.-178+2198G>A
XM_011514617.1:c.-342+2198G>A	XP_011512919.1:n.-342+2198G>A
XM_011514618.1:c.-342+2198G>A	XP_011512920.1:n.-342+2198G>A
XR_926695.1:n.116+9116C>T
NR_149045.1:n.122-2745C>T
XM_011514615.2:c.-342+1000G>A	XP_011512917.1:n.-342+1000G>A
XM_011514616.2:c.-178+2198G>A	XP_011512918.1:n.-178+2198G>A
XM_011514617.2:c.-342+2198G>A	XP_011512919.1:n.-342+2198G>A