Canonical Allele Identifier: CA1290841298
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135833188C= , CM000664.2:g.135833188C= GRCh38
NC_000002.11:g.136590758C= , CM000664.1:g.136590758C= GRCh37
NC_000002.10:g.136307228C= NCBI36
NG_008104.2:g.26982G= , LRG_338:g.26982G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.643G= MANE Select ENSP00000264162.2:p.Gly215=
ENST00000264162.6:c.643G= ENSP00000264162.2:p.Gly215=
NM_002299.2:c.643G= , LRG_338t1:c.643G= NP_002290.2:p.Gly215=
NM_002299.3:c.643G= NP_002290.2:p.Gly215=
XM_017004088.2:c.643G= XP_016859577.1:p.Gly215=
NM_002299.4:c.643G= MANE Select NP_002290.2:p.Gly215=