Canonical Allele Identifier: CA1290834594

Gene: LCT

Linked Data

• dbSNP Id: rs2077785387

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135816961C>T , CM000664.2:g.135816961C>T	GRCh38
NC_000002.11:g.136574531C>T , CM000664.1:g.136574531C>T	GRCh37
NC_000002.10:g.136291001C>T	NCBI36
NG_008104.2:g.43209G>A , LRG_338:g.43209G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.1707+380G>A MANE Select	ENSP00000264162.2:n.1707+380G>A
ENST00000264162.6:c.1707+380G>A	ENSP00000264162.2:n.1707+380G>A
NM_002299.2:c.1707+380G>A , LRG_338t1:c.1707+380G>A	NP_002290.2:n.1707+380G>A
NM_002299.3:c.1707+380G>A	NP_002290.2:n.1707+380G>A
XM_017004088.2:c.1707+380G>A	XP_016859577.1:n.1707+380G>A
NM_002299.4:c.1707+380G>A MANE Select	NP_002290.2:n.1707+380G>A