Canonical Allele Identifier: CA1290821982
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135788072T= , CM000664.2:g.135788072T= GRCh38
NC_000002.11:g.136545642T= , CM000664.1:g.136545642T= GRCh37
NC_000002.10:g.136262112T= NCBI36
NG_008104.2:g.72098A= , LRG_338:g.72098A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*252A= MANE Select ENSP00000264162.2:n.*252A=
ENST00000264162.6:c.*252A= ENSP00000264162.2:n.*252A=
NM_002299.2:c.*252A= , LRG_338t1:c.*252A= NP_002290.2:n.*252A=
NM_002299.3:c.*252A= NP_002290.2:n.*252A=
NM_002299.4:c.*252A= MANE Select NP_002290.2:n.*252A=