Canonical Allele Identifier: CA536394336
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs1235977354

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135797997T>C , CM000664.2:g.135797997T>C GRCh38
NC_000002.11:g.136555567T>C , CM000664.1:g.136555567T>C GRCh37
NC_000002.10:g.136272037T>C NCBI36
NG_008104.2:g.62173A>G , LRG_338:g.62173A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4976+32A>G MANE Select ENSP00000264162.2:n.4976+32A>G
ENST00000264162.6:c.4976+32A>G ENSP00000264162.2:n.4976+32A>G
ENST00000452974.1:c.3069+32A>G ENSP00000391231.1:n.3069+32A>G
NM_002299.2:c.4976+32A>G , LRG_338t1:c.4976+32A>G NP_002290.2:n.4976+32A>G
NM_002299.3:c.4976+32A>G NP_002290.2:n.4976+32A>G
XM_017004088.2:c.4976+32A>G XP_016859577.1:n.4976+32A>G
NM_002299.4:c.4976+32A>G MANE Select NP_002290.2:n.4976+32A>G