Canonical Allele Identifier: CA1087466594
Gene: LTA HGNC NCBI

Linked Data

dbSNP Id: rs1770283307
gnomAD v3: 6-31563481-C-T
gnomAD v4: 6-31563481-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31563481C>T , CM000668.2:g.31563481C>T GRCh38
NC_000006.11:g.31531258C>T , CM000668.1:g.31531258C>T GRCh37
NC_000006.10:g.31639237C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-342+2212C>T XP_011512916.1:n.-342+2212C>T
XM_011514615.1:c.-342+1014C>T XP_011512917.1:n.-342+1014C>T
XM_011514616.1:c.-178+2212C>T XP_011512918.1:n.-178+2212C>T
XM_011514617.1:c.-342+2212C>T XP_011512919.1:n.-342+2212C>T
XM_011514618.1:c.-342+2212C>T XP_011512920.1:n.-342+2212C>T
XR_926695.1:n.116+9102G>A
NR_149045.1:n.122-2759G>A
XM_011514615.2:c.-342+1014C>T XP_011512917.1:n.-342+1014C>T
XM_011514616.2:c.-178+2212C>T XP_011512918.1:n.-178+2212C>T
XM_011514617.2:c.-342+2212C>T XP_011512919.1:n.-342+2212C>T