Canonical Allele Identifier: CA757454297
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs1334487665
gnomAD v3: 2-135789515-C-T
gnomAD v4: 2-135789515-C-T
MyVariant Identifiers: chr2:g.136547085C>T (hg19) chr2:g.135789515C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789515C>T , CM000664.2:g.135789515C>T GRCh38
NC_000002.11:g.136547085C>T , CM000664.1:g.136547085C>T GRCh37
NC_000002.10:g.136263555C>T NCBI36
NG_008104.2:g.70655G>A , LRG_338:g.70655G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.5563+56G>A MANE Select ENSP00000264162.2:n.5563+56G>A
ENST00000264162.6:c.5563+56G>A ENSP00000264162.2:n.5563+56G>A
NM_002299.2:c.5563+56G>A , LRG_338t1:c.5563+56G>A NP_002290.2:n.5563+56G>A
NM_002299.3:c.5563+56G>A NP_002290.2:n.5563+56G>A
NM_002299.4:c.5563+56G>A MANE Select NP_002290.2:n.5563+56G>A
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