Canonical Allele Identifier: CA123913
Gene: LTA HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14379
ClinVar RCV Id: RCV000015455
dbSNP Id: rs1041981

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31573007C>A , CM000668.2:g.31573007C>A GRCh38
NC_000006.11:g.31540784C>A , CM000668.1:g.31540784C>A GRCh37
NC_000006.10:g.31648763C>A NCBI36
NG_007462.1:g.2435C>A
NG_012010.1:g.5909C>A

Transcript Alleles

HGVS Amino-acid change
NM_000595.3:c.179C>A VV NP_000586.2:p.Thr60Asn
NM_001159740.2:c.179C>A VV NP_001153212.1:p.Thr60Asn
XM_011514614.1:c.179C>A XP_011512916.1:p.Thr60Asn
XM_011514615.1:c.179C>A XP_011512917.1:p.Thr60Asn
XM_011514616.1:c.179C>A XP_011512918.1:p.Thr60Asn
XM_011514617.1:c.179C>A XP_011512919.1:p.Thr60Asn
XM_011514618.1:c.179C>A XP_011512920.1:p.Thr60Asn
XM_011514615.2:c.179C>A XP_011512917.1:p.Thr60Asn
XM_011514616.2:c.179C>A XP_011512918.1:p.Thr60Asn
XM_011514617.2:c.179C>A XP_011512919.1:p.Thr60Asn
ENST00000418386.2:c.179C>A ENSP00000413450.2:p.Thr60Asn
ENST00000454783.5:c.179C>A ENSP00000403495.1:p.Thr60Asn
ENST00000471842.1:n.427C>A
ENST00000489638.5:n.307C>A