Canonical Allele Identifier: CA1619210322
Gene: LTA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31565601G>C , CM000668.2:g.31565601G>C GRCh38
NC_000006.11:g.31533378G>C , CM000668.1:g.31533378G>C GRCh37
NC_000006.10:g.31641357G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-342+4332G>C XP_011512916.1:n.-342+4332G>C
XM_011514615.1:c.-342+3134G>C XP_011512917.1:n.-342+3134G>C
XM_011514616.1:c.-178+4332G>C XP_011512918.1:n.-178+4332G>C
XM_011514617.1:c.-342+4332G>C XP_011512919.1:n.-342+4332G>C
XM_011514618.1:c.-342+4332G>C XP_011512920.1:n.-342+4332G>C
XR_926695.1:n.116+6982C>G
NR_149045.1:n.122-4879C>G
XM_011514615.2:c.-342+3134G>C XP_011512917.1:n.-342+3134G>C
XM_011514616.2:c.-178+4332G>C XP_011512918.1:n.-178+4332G>C
XM_011514617.2:c.-342+4332G>C XP_011512919.1:n.-342+4332G>C
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