Canonical Allele Identifier: CA2661276682
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135833084A>C , CM000664.2:g.135833084A>C GRCh38
NC_000002.11:g.136590654A>C , CM000664.1:g.136590654A>C GRCh37
NC_000002.10:g.136307124A>C NCBI36
NG_008104.2:g.27086T>G , LRG_338:g.27086T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.720+27T>G MANE Select ENSP00000264162.2:n.720+27T>G
ENST00000264162.6:c.720+27T>G ENSP00000264162.2:n.720+27T>G
NM_002299.2:c.720+27T>G , LRG_338t1:c.720+27T>G NP_002290.2:n.720+27T>G
NM_002299.3:c.720+27T>G NP_002290.2:n.720+27T>G
XM_017004088.2:c.720+27T>G XP_016859577.1:n.720+27T>G
NM_002299.4:c.720+27T>G MANE Select NP_002290.2:n.720+27T>G