Canonical Allele Identifier: CA56602861
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs557453746

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135798206C>T , CM000664.2:g.135798206C>T GRCh38
NC_000002.11:g.136555776C>T , CM000664.1:g.136555776C>T GRCh37
NC_000002.10:g.136272246C>T NCBI36
NG_008104.2:g.61964G>A , LRG_338:g.61964G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.4867-68G>A MANE Select ENSP00000264162.2:n.4867-68G>A
ENST00000264162.6:c.4867-68G>A ENSP00000264162.2:n.4867-68G>A
ENST00000452974.1:c.2960-68G>A ENSP00000391231.1:n.2960-68G>A
NM_002299.2:c.4867-68G>A , LRG_338t1:c.4867-68G>A NP_002290.2:n.4867-68G>A
NM_002299.3:c.4867-68G>A NP_002290.2:n.4867-68G>A
XM_017004088.2:c.4867-68G>A XP_016859577.1:n.4867-68G>A
NM_002299.4:c.4867-68G>A MANE Select NP_002290.2:n.4867-68G>A