Canonical Allele Identifier: CA348586308
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789654G>C , CM000664.2:g.135789654G>C GRCh38
NC_000002.11:g.136547224G>C , CM000664.1:g.136547224G>C GRCh37
NC_000002.10:g.136263694G>C NCBI36
NG_008104.2:g.70516C>G , LRG_338:g.70516C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.5480C>G MANE Select ENSP00000264162.2:p.Ser1827Ter
ENST00000264162.6:c.5480C>G ENSP00000264162.2:p.Ser1827Ter
NM_002299.2:c.5480C>G , LRG_338t1:c.5480C>G NP_002290.2:p.Ser1827Ter
NM_002299.3:c.5480C>G NP_002290.2:p.Ser1827Ter
NM_002299.4:c.5480C>G MANE Select NP_002290.2:p.Ser1827Ter