Canonical Allele Identifier: CA1087466604
Gene: LTA HGNC NCBI

Linked Data

dbSNP Id: rs1770284961
gnomAD v3: 6-31563502-G-C
gnomAD v4: 6-31563502-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31563502G>C , CM000668.2:g.31563502G>C GRCh38
NC_000006.11:g.31531279G>C , CM000668.1:g.31531279G>C GRCh37
NC_000006.10:g.31639258G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-342+2233G>C XP_011512916.1:n.-342+2233G>C
XM_011514615.1:c.-342+1035G>C XP_011512917.1:n.-342+1035G>C
XM_011514616.1:c.-178+2233G>C XP_011512918.1:n.-178+2233G>C
XM_011514617.1:c.-342+2233G>C XP_011512919.1:n.-342+2233G>C
XM_011514618.1:c.-342+2233G>C XP_011512920.1:n.-342+2233G>C
XR_926695.1:n.116+9081C>G
NR_149045.1:n.122-2780C>G
XM_011514615.2:c.-342+1035G>C XP_011512917.1:n.-342+1035G>C
XM_011514616.2:c.-178+2233G>C XP_011512918.1:n.-178+2233G>C
XM_011514617.2:c.-342+2233G>C XP_011512919.1:n.-342+2233G>C