Canonical Allele Identifier: CA348608851
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135833179A>C , CM000664.2:g.135833179A>C GRCh38
NC_000002.11:g.136590749A>C , CM000664.1:g.136590749A>C GRCh37
NC_000002.10:g.136307219A>C NCBI36
NG_008104.2:g.26991T>G , LRG_338:g.26991T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.652T>G MANE Select ENSP00000264162.2:p.Ser218Ala
ENST00000264162.6:c.652T>G ENSP00000264162.2:p.Ser218Ala
NM_002299.2:c.652T>G , LRG_338t1:c.652T>G NP_002290.2:p.Ser218Ala
NM_002299.3:c.652T>G NP_002290.2:p.Ser218Ala
XM_017004088.2:c.652T>G XP_016859577.1:p.Ser218Ala
NM_002299.4:c.652T>G MANE Select NP_002290.2:p.Ser218Ala