Canonical Allele Identifier: CA1887606
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 331166
dbSNP Id: rs369410973

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789641G>A , CM000664.2:g.135789641G>A GRCh38
NC_000002.11:g.136547211G>A , CM000664.1:g.136547211G>A GRCh37
NC_000002.10:g.136263681G>A NCBI36
NG_008104.2:g.70529C>T , LRG_338:g.70529C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.5493C>T MANE Select ENSP00000264162.2:p.Tyr1831=
ENST00000264162.6:c.5493C>T ENSP00000264162.2:p.Tyr1831=
NM_002299.2:c.5493C>T , LRG_338t1:c.5493C>T NP_002290.2:p.Tyr1831=
NM_002299.3:c.5493C>T NP_002290.2:p.Tyr1831=
NM_002299.4:c.5493C>T MANE Select NP_002290.2:p.Tyr1831=