Canonical Allele Identifier: CA1619210711
Gene: LTA HGNC NCBI

Linked Data

dbSNP Id: rs2844484
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31568447A>C , CM000668.2:g.31568447A>C GRCh38
NC_000006.11:g.31536224A>C , CM000668.1:g.31536224A>C GRCh37
NC_000006.10:g.31644203A>C NCBI36
NG_012010.1:g.1349A>C

Transcript Alleles

HGVS Amino-acid change
XM_011514614.1:c.-341-3045A>C XP_011512916.1:n.-341-3045A>C
XM_011514615.1:c.-341-3045A>C XP_011512917.1:n.-341-3045A>C
XM_011514616.1:c.-177-3688A>C XP_011512918.1:n.-177-3688A>C
XM_011514617.1:c.-341-3045A>C XP_011512919.1:n.-341-3045A>C
XM_011514618.1:c.-341-3045A>C XP_011512920.1:n.-341-3045A>C
XR_926695.1:n.116+4136T>G
NR_149045.1:n.121+4136T>G
XM_011514615.2:c.-341-3045A>C XP_011512917.1:n.-341-3045A>C
XM_011514616.2:c.-177-3688A>C XP_011512918.1:n.-177-3688A>C
XM_011514617.2:c.-341-3045A>C XP_011512919.1:n.-341-3045A>C
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