Canonical Allele Identifier: CA2661271109
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135787908-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787908C>T , CM000664.2:g.135787908C>T GRCh38
NC_000002.11:g.136545478C>T , CM000664.1:g.136545478C>T GRCh37
NC_000002.10:g.136261948C>T NCBI36
NG_008104.2:g.72262G>A , LRG_338:g.72262G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*416G>A MANE Select ENSP00000264162.2:n.*416G>A
ENST00000264162.6:c.*416G>A ENSP00000264162.2:n.*416G>A
NM_002299.2:c.*416G>A , LRG_338t1:c.*416G>A NP_002290.2:n.*416G>A
NM_002299.3:c.*416G>A NP_002290.2:n.*416G>A
NM_002299.4:c.*416G>A MANE Select NP_002290.2:n.*416G>A
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