Canonical Allele Identifier: CA348608852
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.652T>C MANE Select ENSP00000264162.2:p.Ser218Pro
ENST00000264162.6:c.652T>C ENSP00000264162.2:p.Ser218Pro
NM_002299.2:c.652T>C , LRG_338t1:c.652T>C NP_002290.2:p.Ser218Pro
NM_002299.3:c.652T>C NP_002290.2:p.Ser218Pro
XM_017004088.2:c.652T>C XP_016859577.1:p.Ser218Pro
NM_002299.4:c.652T>C MANE Select NP_002290.2:p.Ser218Pro