Canonical Allele Identifier: CA1619211483
Gene: LTA HGNC NCBI

Linked Data

dbSNP Id: rs1770776268

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31570564T>G , CM000668.2:g.31570564T>G GRCh38
NC_000006.11:g.31538341T>G , CM000668.1:g.31538341T>G GRCh37
NC_000006.10:g.31646320T>G NCBI36
NG_012010.1:g.3466T>G

Transcript Alleles

HGVS Amino-acid change
XM_011514614.1:c.-341-928T>G XP_011512916.1:n.-341-928T>G
XM_011514615.1:c.-341-928T>G XP_011512917.1:n.-341-928T>G
XM_011514616.1:c.-177-1571T>G XP_011512918.1:n.-177-1571T>G
XM_011514617.1:c.-341-928T>G XP_011512919.1:n.-341-928T>G
XM_011514618.1:c.-341-928T>G XP_011512920.1:n.-341-928T>G
XR_926695.1:n.116+2019A>C
NR_149045.1:n.121+2019A>C
XM_011514615.2:c.-341-928T>G XP_011512917.1:n.-341-928T>G
XM_011514616.2:c.-177-1571T>G XP_011512918.1:n.-177-1571T>G
XM_011514617.2:c.-341-928T>G XP_011512919.1:n.-341-928T>G