Canonical Allele Identifier: CA136856014

Gene: LTA

Linked Data

• dbSNP Id: rs892607358
• MyVariant Identifiers: chr6:g.31531293A>G (hg19) ; chr6:g.31563516A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31563516A>G , CM000668.2:g.31563516A>G	GRCh38
NC_000006.11:g.31531293A>G , CM000668.1:g.31531293A>G	GRCh37
NC_000006.10:g.31639272A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011514614.1:c.-342+2247A>G	XP_011512916.1:n.-342+2247A>G
XM_011514615.1:c.-342+1049A>G	XP_011512917.1:n.-342+1049A>G
XM_011514616.1:c.-178+2247A>G	XP_011512918.1:n.-178+2247A>G
XM_011514617.1:c.-342+2247A>G	XP_011512919.1:n.-342+2247A>G
XM_011514618.1:c.-342+2247A>G	XP_011512920.1:n.-342+2247A>G
XR_926695.1:n.116+9067T>C
NR_149045.1:n.122-2794T>C
XM_011514615.2:c.-342+1049A>G	XP_011512917.1:n.-342+1049A>G
XM_011514616.2:c.-178+2247A>G	XP_011512918.1:n.-178+2247A>G
XM_011514617.2:c.-342+2247A>G	XP_011512919.1:n.-342+2247A>G