Canonical Allele Identifier: CA5330626
Community Standard Title: NM_178138.6(LHX3):c.79+1935C>G
Gene: LHX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136202999G>C , CM000671.2:g.136202999G>C GRCh38
NC_000009.11:g.139094845G>C , CM000671.1:g.139094845G>C GRCh37
NC_000009.10:g.138234666G>C NCBI36
NG_008097.1:g.7111C>G

Transcript Alleles

HGVS Amino-acid Change
NM_178138.6:c.79+1935C>G MANE Select NP_835258.1:n.79+1935C>G
ENST00000371748.10:c.79+1935C>G MANE Select ENSP00000360813.4:n.79+1935C>G
NM_014564.3:c.41C>G NP_055379.1:p.Ala14Gly
NM_014564.4:c.41C>G NP_055379.1:p.Ala14Gly
NM_014564.5:c.41C>G NP_055379.1:p.Ala14Gly
NM_178138.4:c.79+1935C>G NP_835258.1:n.79+1935C>G
NM_178138.5:c.79+1935C>G NP_835258.1:n.79+1935C>G
ENST00000371746.7:c.41C>G ENSP00000360811.3:p.Ala14Gly
ENST00000371746.9:c.41C>G ENSP00000360811.3:p.Ala14Gly
ENST00000371748.9:c.79+1935C>G ENSP00000360813.4:n.79+1935C>G
ENST00000645419.1:n.150C>G