Canonical Allele Identifier: CA2661274796
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135800526-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135800526C>T , CM000664.2:g.135800526C>T GRCh38
NC_000002.11:g.136558096C>T , CM000664.1:g.136558096C>T GRCh37
NC_000002.10:g.136274566C>T NCBI36
NG_008104.2:g.59644G>A , LRG_338:g.59644G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.4866+81G>A MANE Select ENSP00000264162.2:n.4866+81G>A
ENST00000264162.6:c.4866+81G>A ENSP00000264162.2:n.4866+81G>A
ENST00000452974.1:c.2960-2388G>A ENSP00000391231.1:n.2960-2388G>A
NM_002299.2:c.4866+81G>A , LRG_338t1:c.4866+81G>A NP_002290.2:n.4866+81G>A
NM_002299.3:c.4866+81G>A NP_002290.2:n.4866+81G>A
XM_017004088.2:c.4866+81G>A XP_016859577.1:n.4866+81G>A
NM_002299.4:c.4866+81G>A MANE Select NP_002290.2:n.4866+81G>A
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