Canonical Allele Identifier: CA348586471

Gene: LCT

Linked Data

• MyVariant Identifiers: chr2:g.136547263T>A (hg19) ; chr2:g.135789693T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135789693T>A , CM000664.2:g.135789693T>A	GRCh38
NC_000002.11:g.136547263T>A , CM000664.1:g.136547263T>A	GRCh37
NC_000002.10:g.136263733T>A	NCBI36
NG_008104.2:g.70477A>T , LRG_338:g.70477A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5441A>T MANE Select	ENSP00000264162.2:p.Asn1814Ile
ENST00000264162.6:c.5441A>T	ENSP00000264162.2:p.Asn1814Ile
NM_002299.2:c.5441A>T , LRG_338t1:c.5441A>T	NP_002290.2:p.Asn1814Ile
NM_002299.3:c.5441A>T	NP_002290.2:p.Asn1814Ile
NM_002299.4:c.5441A>T MANE Select	NP_002290.2:p.Asn1814Ile