Canonical Allele Identifier: CA1290822828
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs2077521663
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135790035A>T , CM000664.2:g.135790035A>T GRCh38
NC_000002.11:g.136547605A>T , CM000664.1:g.136547605A>T GRCh37
NC_000002.10:g.136264075A>T NCBI36
NG_008104.2:g.70135T>A , LRG_338:g.70135T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.5336-237T>A MANE Select ENSP00000264162.2:n.5336-237T>A
ENST00000264162.6:c.5336-237T>A ENSP00000264162.2:n.5336-237T>A
NM_002299.2:c.5336-237T>A , LRG_338t1:c.5336-237T>A NP_002290.2:n.5336-237T>A
NM_002299.3:c.5336-237T>A NP_002290.2:n.5336-237T>A
NM_002299.4:c.5336-237T>A MANE Select NP_002290.2:n.5336-237T>A
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