Canonical Allele Identifier: CA56595378
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs938791423
gnomAD v3: 2-135790000-G-C
gnomAD v4: 2-135790000-G-C
MyVariant Identifiers: chr2:g.136547570G>C (hg19) chr2:g.135790000G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135790000G>C , CM000664.2:g.135790000G>C GRCh38
NC_000002.11:g.136547570G>C , CM000664.1:g.136547570G>C GRCh37
NC_000002.10:g.136264040G>C NCBI36
NG_008104.2:g.70170C>G , LRG_338:g.70170C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.5336-202C>G MANE Select ENSP00000264162.2:n.5336-202C>G
ENST00000264162.6:c.5336-202C>G ENSP00000264162.2:n.5336-202C>G
NM_002299.2:c.5336-202C>G , LRG_338t1:c.5336-202C>G NP_002290.2:n.5336-202C>G
NM_002299.3:c.5336-202C>G NP_002290.2:n.5336-202C>G
NM_002299.4:c.5336-202C>G MANE Select NP_002290.2:n.5336-202C>G
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