Canonical Allele Identifier: CA2661271137
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135787934-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787934T>A , CM000664.2:g.135787934T>A GRCh38
NC_000002.11:g.136545504T>A , CM000664.1:g.136545504T>A GRCh37
NC_000002.10:g.136261974T>A NCBI36
NG_008104.2:g.72236A>T , LRG_338:g.72236A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.*390A>T MANE Select ENSP00000264162.2:n.*390A>T
ENST00000264162.6:c.*390A>T ENSP00000264162.2:n.*390A>T
NM_002299.2:c.*390A>T , LRG_338t1:c.*390A>T NP_002290.2:n.*390A>T
NM_002299.3:c.*390A>T NP_002290.2:n.*390A>T
NM_002299.4:c.*390A>T MANE Select NP_002290.2:n.*390A>T
Search 100 bp 5'
Search 100 bp 3'