Canonical Allele Identifier: CA136856000

Gene: LTA

Linked Data

• dbSNP Id: rs142103600
• gnomAD v3: 6-31563452-G-A
• gnomAD v4: 6-31563452-G-A
• MyVariant Identifiers: chr6:g.31531229G>A (hg19) ; chr6:g.31563452G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31563452G>A , CM000668.2:g.31563452G>A	GRCh38
NC_000006.11:g.31531229G>A , CM000668.1:g.31531229G>A	GRCh37
NC_000006.10:g.31639208G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011514614.1:c.-342+2183G>A	XP_011512916.1:n.-342+2183G>A
XM_011514615.1:c.-342+985G>A	XP_011512917.1:n.-342+985G>A
XM_011514616.1:c.-178+2183G>A	XP_011512918.1:n.-178+2183G>A
XM_011514617.1:c.-342+2183G>A	XP_011512919.1:n.-342+2183G>A
XM_011514618.1:c.-342+2183G>A	XP_011512920.1:n.-342+2183G>A
XR_926695.1:n.116+9131C>T
NR_149045.1:n.122-2730C>T
XM_011514615.2:c.-342+985G>A	XP_011512917.1:n.-342+985G>A
XM_011514616.2:c.-178+2183G>A	XP_011512918.1:n.-178+2183G>A
XM_011514617.2:c.-342+2183G>A	XP_011512919.1:n.-342+2183G>A