Canonical Allele Identifier: CA1619211554
Gene: LTA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31570720T>C , CM000668.2:g.31570720T>C GRCh38
NC_000006.11:g.31538497T>C , CM000668.1:g.31538497T>C GRCh37
NC_000006.10:g.31646476T>C NCBI36
NG_007462.1:g.148T>C
NG_012010.1:g.3622T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011514614.1:c.-341-772T>C XP_011512916.1:n.-341-772T>C
XM_011514615.1:c.-341-772T>C XP_011512917.1:n.-341-772T>C
XM_011514616.1:c.-177-1415T>C XP_011512918.1:n.-177-1415T>C
XM_011514617.1:c.-341-772T>C XP_011512919.1:n.-341-772T>C
XM_011514618.1:c.-341-772T>C XP_011512920.1:n.-341-772T>C
XR_926695.1:n.116+1863A>G
NR_149045.1:n.121+1863A>G
XM_011514615.2:c.-341-772T>C XP_011512917.1:n.-341-772T>C
XM_011514616.2:c.-177-1415T>C XP_011512918.1:n.-177-1415T>C
XM_011514617.2:c.-341-772T>C XP_011512919.1:n.-341-772T>C
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