Canonical Allele Identifier: CA12266078
Gene: LTA HGNC NCBI

Linked Data

dbSNP Id: rs2857708
gnomAD v2: 6-31533606-C-T
gnomAD v3: 6-31565829-C-T
gnomAD v4: 6-31565829-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31565829C>T , CM000668.2:g.31565829C>T GRCh38
NC_000006.11:g.31533606C>T , CM000668.1:g.31533606C>T GRCh37
NC_000006.10:g.31641585C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-342+4560C>T XP_011512916.1:n.-342+4560C>T
XM_011514615.1:c.-342+3362C>T XP_011512917.1:n.-342+3362C>T
XM_011514616.1:c.-178+4560C>T XP_011512918.1:n.-178+4560C>T
XM_011514617.1:c.-342+4560C>T XP_011512919.1:n.-342+4560C>T
XM_011514618.1:c.-342+4560C>T XP_011512920.1:n.-342+4560C>T
XR_926695.1:n.116+6754G>A
NR_149045.1:n.122-5107G>A
XM_011514615.2:c.-342+3362C>T XP_011512917.1:n.-342+3362C>T
XM_011514616.2:c.-178+4560C>T XP_011512918.1:n.-178+4560C>T
XM_011514617.2:c.-342+4560C>T XP_011512919.1:n.-342+4560C>T