Canonical Allele Identifier: CA1619211430
Gene: LTA HGNC NCBI

Linked Data

dbSNP Id: rs1770769622

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31570402C>T , CM000668.2:g.31570402C>T GRCh38
NC_000006.11:g.31538179C>T , CM000668.1:g.31538179C>T GRCh37
NC_000006.10:g.31646158C>T NCBI36
NG_012010.1:g.3304C>T

Transcript Alleles

HGVS Amino-acid change
XM_011514614.1:c.-341-1090C>T XP_011512916.1:n.-341-1090C>T
XM_011514615.1:c.-341-1090C>T XP_011512917.1:n.-341-1090C>T
XM_011514616.1:c.-177-1733C>T XP_011512918.1:n.-177-1733C>T
XM_011514617.1:c.-341-1090C>T XP_011512919.1:n.-341-1090C>T
XM_011514618.1:c.-341-1090C>T XP_011512920.1:n.-341-1090C>T
XR_926695.1:n.116+2181G>A
NR_149045.1:n.121+2181G>A
XM_011514615.2:c.-341-1090C>T XP_011512917.1:n.-341-1090C>T
XM_011514616.2:c.-177-1733C>T XP_011512918.1:n.-177-1733C>T
XM_011514617.2:c.-341-1090C>T XP_011512919.1:n.-341-1090C>T