Canonical Allele Identifier: CA2661271250
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135788058-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135788058C>A , CM000664.2:g.135788058C>A GRCh38
NC_000002.11:g.136545628C>A , CM000664.1:g.136545628C>A GRCh37
NC_000002.10:g.136262098C>A NCBI36
NG_008104.2:g.72112G>T , LRG_338:g.72112G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*266G>T MANE Select ENSP00000264162.2:n.*266G>T
ENST00000264162.6:c.*266G>T ENSP00000264162.2:n.*266G>T
NM_002299.2:c.*266G>T , LRG_338t1:c.*266G>T NP_002290.2:n.*266G>T
NM_002299.3:c.*266G>T NP_002290.2:n.*266G>T
NM_002299.4:c.*266G>T MANE Select NP_002290.2:n.*266G>T
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