Canonical Allele Identifier: CA1290821937
Gene: LCT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787957T= , CM000664.2:g.135787957T= GRCh38
NC_000002.11:g.136545527T= , CM000664.1:g.136545527T= GRCh37
NC_000002.10:g.136261997T= NCBI36
NG_008104.2:g.72213A= , LRG_338:g.72213A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.*367A= MANE Select ENSP00000264162.2:n.*367A=
ENST00000264162.6:c.*367A= ENSP00000264162.2:n.*367A=
NM_002299.2:c.*367A= , LRG_338t1:c.*367A= NP_002290.2:n.*367A=
NM_002299.3:c.*367A= NP_002290.2:n.*367A=
NM_002299.4:c.*367A= MANE Select NP_002290.2:n.*367A=
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