Canonical Allele Identifier: CA429086451
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135800739-G-C
MyVariant Identifiers: chr2:g.136558309G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135800739G>C , CM000664.2:g.135800739G>C GRCh38
NC_000002.11:g.136558309G>C , CM000664.1:g.136558309G>C GRCh37
NC_000002.10:g.136274779G>C NCBI36
NG_008104.2:g.59431C>G , LRG_338:g.59431C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.4734C>G MANE Select ENSP00000264162.2:p.Ala1578=
ENST00000264162.6:c.4734C>G ENSP00000264162.2:p.Ala1578=
ENST00000452974.1:c.2960-2601C>G ENSP00000391231.1:n.2960-2601C>G
NM_002299.2:c.4734C>G , LRG_338t1:c.4734C>G NP_002290.2:p.Ala1578=
NM_002299.3:c.4734C>G NP_002290.2:p.Ala1578=
XM_017004088.2:c.4734C>G XP_016859577.1:p.Ala1578=
NM_002299.4:c.4734C>G MANE Select NP_002290.2:p.Ala1578=
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