Canonical Allele Identifier: CA2700409488

Gene: LCT

Linked Data

• dbSNP Id: rs891720069

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135817202G>C , CM000664.2:g.135817202G>C	GRCh38
NC_000002.11:g.136574772G>C , CM000664.1:g.136574772G>C	GRCh37
NC_000002.10:g.136291242G>C	NCBI36
NG_008104.2:g.42968C>G , LRG_338:g.42968C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264162.7:c.1707+139C>G MANE Select	ENSP00000264162.2:n.1707+139C>G
ENST00000264162.6:c.1707+139C>G	ENSP00000264162.2:n.1707+139C>G
NM_002299.2:c.1707+139C>G , LRG_338t1:c.1707+139C>G	NP_002290.2:n.1707+139C>G
NM_002299.3:c.1707+139C>G	NP_002290.2:n.1707+139C>G
XM_017004088.2:c.1707+139C>G	XP_016859577.1:n.1707+139C>G
NM_002299.4:c.1707+139C>G MANE Select	NP_002290.2:n.1707+139C>G