Canonical Allele Identifier: CA2661271136
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135787933-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787933G>C , CM000664.2:g.135787933G>C GRCh38
NC_000002.11:g.136545503G>C , CM000664.1:g.136545503G>C GRCh37
NC_000002.10:g.136261973G>C NCBI36
NG_008104.2:g.72237C>G , LRG_338:g.72237C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*391C>G MANE Select ENSP00000264162.2:n.*391C>G
ENST00000264162.6:c.*391C>G ENSP00000264162.2:n.*391C>G
NM_002299.2:c.*391C>G , LRG_338t1:c.*391C>G NP_002290.2:n.*391C>G
NM_002299.3:c.*391C>G NP_002290.2:n.*391C>G
NM_002299.4:c.*391C>G MANE Select NP_002290.2:n.*391C>G
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