Canonical Allele Identifier: CA823888564

Gene: LTA

Linked Data

• dbSNP Id: rs1221521814
• gnomAD v3: 6-31570413-G-C
• gnomAD v4: 6-31570413-G-C
• MyVariant Identifiers: chr6:g.31538190G>C (hg19) ; chr6:g.31570413G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31570413G>C , CM000668.2:g.31570413G>C	GRCh38
NC_000006.11:g.31538190G>C , CM000668.1:g.31538190G>C	GRCh37
NC_000006.10:g.31646169G>C	NCBI36
NG_012010.1:g.3315G>C

Transcript Alleles

HGVS	Amino-acid change
XM_011514614.1:c.-341-1079G>C	XP_011512916.1:n.-341-1079G>C
XM_011514615.1:c.-341-1079G>C	XP_011512917.1:n.-341-1079G>C
XM_011514616.1:c.-177-1722G>C	XP_011512918.1:n.-177-1722G>C
XM_011514617.1:c.-341-1079G>C	XP_011512919.1:n.-341-1079G>C
XM_011514618.1:c.-341-1079G>C	XP_011512920.1:n.-341-1079G>C
XR_926695.1:n.116+2170C>G
NR_149045.1:n.121+2170C>G
XM_011514615.2:c.-341-1079G>C	XP_011512917.1:n.-341-1079G>C
XM_011514616.2:c.-177-1722G>C	XP_011512918.1:n.-177-1722G>C
XM_011514617.2:c.-341-1079G>C	XP_011512919.1:n.-341-1079G>C