Canonical Allele Identifier: CA348586485
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789699A>T , CM000664.2:g.135789699A>T GRCh38
NC_000002.11:g.136547269A>T , CM000664.1:g.136547269A>T GRCh37
NC_000002.10:g.136263739A>T NCBI36
NG_008104.2:g.70471T>A , LRG_338:g.70471T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.5435T>A MANE Select ENSP00000264162.2:p.Phe1812Tyr
ENST00000264162.6:c.5435T>A ENSP00000264162.2:p.Phe1812Tyr
NM_002299.2:c.5435T>A , LRG_338t1:c.5435T>A NP_002290.2:p.Phe1812Tyr
NM_002299.3:c.5435T>A NP_002290.2:p.Phe1812Tyr
NM_002299.4:c.5435T>A MANE Select NP_002290.2:p.Phe1812Tyr