Canonical Allele Identifier: CA1619211476
Gene: LTA HGNC NCBI

Linked Data

dbSNP Id: rs1770775459
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31570548T>A , CM000668.2:g.31570548T>A GRCh38
NC_000006.11:g.31538325T>A , CM000668.1:g.31538325T>A GRCh37
NC_000006.10:g.31646304T>A NCBI36
NG_012010.1:g.3450T>A

Transcript Alleles

HGVS Amino-acid change
XM_011514614.1:c.-341-944T>A XP_011512916.1:n.-341-944T>A
XM_011514615.1:c.-341-944T>A XP_011512917.1:n.-341-944T>A
XM_011514616.1:c.-177-1587T>A XP_011512918.1:n.-177-1587T>A
XM_011514617.1:c.-341-944T>A XP_011512919.1:n.-341-944T>A
XM_011514618.1:c.-341-944T>A XP_011512920.1:n.-341-944T>A
XR_926695.1:n.116+2035A>T
NR_149045.1:n.121+2035A>T
XM_011514615.2:c.-341-944T>A XP_011512917.1:n.-341-944T>A
XM_011514616.2:c.-177-1587T>A XP_011512918.1:n.-177-1587T>A
XM_011514617.2:c.-341-944T>A XP_011512919.1:n.-341-944T>A
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