Canonical Allele Identifier: CA2661276657
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135833016A>G , CM000664.2:g.135833016A>G GRCh38
NC_000002.11:g.136590586A>G , CM000664.1:g.136590586A>G GRCh37
NC_000002.10:g.136307056A>G NCBI36
NG_008104.2:g.27154T>C , LRG_338:g.27154T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.720+95T>C MANE Select ENSP00000264162.2:n.720+95T>C
ENST00000264162.6:c.720+95T>C ENSP00000264162.2:n.720+95T>C
NM_002299.2:c.720+95T>C , LRG_338t1:c.720+95T>C NP_002290.2:n.720+95T>C
NM_002299.3:c.720+95T>C NP_002290.2:n.720+95T>C
XM_017004088.2:c.720+95T>C XP_016859577.1:n.720+95T>C
NM_002299.4:c.720+95T>C MANE Select NP_002290.2:n.720+95T>C