Canonical Allele Identifier: CA2661273560
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135789559-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789559G>T , CM000664.2:g.135789559G>T GRCh38
NC_000002.11:g.136547129G>T , CM000664.1:g.136547129G>T GRCh37
NC_000002.10:g.136263599G>T NCBI36
NG_008104.2:g.70611C>A , LRG_338:g.70611C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.5563+12C>A MANE Select ENSP00000264162.2:n.5563+12C>A
ENST00000264162.6:c.5563+12C>A ENSP00000264162.2:n.5563+12C>A
NM_002299.2:c.5563+12C>A , LRG_338t1:c.5563+12C>A NP_002290.2:n.5563+12C>A
NM_002299.3:c.5563+12C>A NP_002290.2:n.5563+12C>A
NM_002299.4:c.5563+12C>A MANE Select NP_002290.2:n.5563+12C>A
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