Canonical Allele Identifier: CA56593524

Gene: LCT

Linked Data

• dbSNP Id: rs970403399
• MyVariant Identifiers: chr2:g.136545535G>A (hg19) ; chr2:g.135787965G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135787965G>A , CM000664.2:g.135787965G>A	GRCh38
NC_000002.11:g.136545535G>A , CM000664.1:g.136545535G>A	GRCh37
NC_000002.10:g.136262005G>A	NCBI36
NG_008104.2:g.72205C>T , LRG_338:g.72205C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.*359C>T MANE Select	ENSP00000264162.2:n.*359C>T
ENST00000264162.6:c.*359C>T	ENSP00000264162.2:n.*359C>T
NM_002299.2:c.*359C>T , LRG_338t1:c.*359C>T	NP_002290.2:n.*359C>T
NM_002299.3:c.*359C>T	NP_002290.2:n.*359C>T
NM_002299.4:c.*359C>T MANE Select	NP_002290.2:n.*359C>T