Canonical Allele Identifier: CA1290834732
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs2077787755
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135817317A>G , CM000664.2:g.135817317A>G GRCh38
NC_000002.11:g.136574887A>G , CM000664.1:g.136574887A>G GRCh37
NC_000002.10:g.136291357A>G NCBI36
NG_008104.2:g.42853T>C , LRG_338:g.42853T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.1707+24T>C MANE Select ENSP00000264162.2:n.1707+24T>C
ENST00000264162.6:c.1707+24T>C ENSP00000264162.2:n.1707+24T>C
NM_002299.2:c.1707+24T>C , LRG_338t1:c.1707+24T>C NP_002290.2:n.1707+24T>C
NM_002299.3:c.1707+24T>C NP_002290.2:n.1707+24T>C
XM_017004088.2:c.1707+24T>C XP_016859577.1:n.1707+24T>C
NM_002299.4:c.1707+24T>C MANE Select NP_002290.2:n.1707+24T>C
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