Canonical Allele Identifier: CA2661271085
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135787900-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787900A>C , CM000664.2:g.135787900A>C GRCh38
NC_000002.11:g.136545470A>C , CM000664.1:g.136545470A>C GRCh37
NC_000002.10:g.136261940A>C NCBI36
NG_008104.2:g.72270T>G , LRG_338:g.72270T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*424T>G MANE Select ENSP00000264162.2:n.*424T>G
ENST00000264162.6:c.*424T>G ENSP00000264162.2:n.*424T>G
NM_002299.2:c.*424T>G , LRG_338t1:c.*424T>G NP_002290.2:n.*424T>G
NM_002299.3:c.*424T>G NP_002290.2:n.*424T>G
NM_002299.4:c.*424T>G MANE Select NP_002290.2:n.*424T>G
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