Canonical Allele Identifier: CA348586278
Gene: LCT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.136547219T>A (hg19) chr2:g.135789649T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789649T>A , CM000664.2:g.135789649T>A GRCh38
NC_000002.11:g.136547219T>A , CM000664.1:g.136547219T>A GRCh37
NC_000002.10:g.136263689T>A NCBI36
NG_008104.2:g.70521A>T , LRG_338:g.70521A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.5485A>T MANE Select ENSP00000264162.2:p.Lys1829Ter
ENST00000264162.6:c.5485A>T ENSP00000264162.2:p.Lys1829Ter
NM_002299.2:c.5485A>T , LRG_338t1:c.5485A>T NP_002290.2:p.Lys1829Ter
NM_002299.3:c.5485A>T NP_002290.2:p.Lys1829Ter
NM_002299.4:c.5485A>T MANE Select NP_002290.2:p.Lys1829Ter
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