Canonical Allele Identifier: CA1290841181

Gene: LCT

Linked Data

• dbSNP Id: rs2077950968

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135832834A>C , CM000664.2:g.135832834A>C	GRCh38
NC_000002.11:g.136590404A>C , CM000664.1:g.136590404A>C	GRCh37
NC_000002.10:g.136306874A>C	NCBI36
NG_008104.2:g.27336T>G , LRG_338:g.27336T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.720+277T>G MANE Select	ENSP00000264162.2:n.720+277T>G
ENST00000264162.6:c.720+277T>G	ENSP00000264162.2:n.720+277T>G
NM_002299.2:c.720+277T>G , LRG_338t1:c.720+277T>G	NP_002290.2:n.720+277T>G
NM_002299.3:c.720+277T>G	NP_002290.2:n.720+277T>G
XM_017004088.2:c.720+277T>G	XP_016859577.1:n.720+277T>G
NM_002299.4:c.720+277T>G MANE Select	NP_002290.2:n.720+277T>G