Canonical Allele Identifier: CA1290821938
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs2077504713

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787957T>A , CM000664.2:g.135787957T>A GRCh38
NC_000002.11:g.136545527T>A , CM000664.1:g.136545527T>A GRCh37
NC_000002.10:g.136261997T>A NCBI36
NG_008104.2:g.72213A>T , LRG_338:g.72213A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*367A>T MANE Select ENSP00000264162.2:n.*367A>T
ENST00000264162.6:c.*367A>T ENSP00000264162.2:n.*367A>T
NM_002299.2:c.*367A>T , LRG_338t1:c.*367A>T NP_002290.2:n.*367A>T
NM_002299.3:c.*367A>T NP_002290.2:n.*367A>T
NM_002299.4:c.*367A>T MANE Select NP_002290.2:n.*367A>T