Canonical Allele Identifier: CA566350965

Gene: LTA

Linked Data

• dbSNP Id: rs1425928719
• gnomAD v2: 6-31531332-A-C
• gnomAD v3: 6-31563555-A-C
• gnomAD v4: 6-31563555-A-C
• MyVariant Identifiers: chr6:g.31531332A>C (hg19) ; chr6:g.31563555A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31563555A>C , CM000668.2:g.31563555A>C	GRCh38
NC_000006.11:g.31531332A>C , CM000668.1:g.31531332A>C	GRCh37
NC_000006.10:g.31639311A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011514614.1:c.-342+2286A>C	XP_011512916.1:n.-342+2286A>C
XM_011514615.1:c.-342+1088A>C	XP_011512917.1:n.-342+1088A>C
XM_011514616.1:c.-178+2286A>C	XP_011512918.1:n.-178+2286A>C
XM_011514617.1:c.-342+2286A>C	XP_011512919.1:n.-342+2286A>C
XM_011514618.1:c.-342+2286A>C	XP_011512920.1:n.-342+2286A>C
XR_926695.1:n.116+9028T>G
NR_149045.1:n.122-2833T>G
XM_011514615.2:c.-342+1088A>C	XP_011512917.1:n.-342+1088A>C
XM_011514616.2:c.-178+2286A>C	XP_011512918.1:n.-178+2286A>C
XM_011514617.2:c.-342+2286A>C	XP_011512919.1:n.-342+2286A>C