Canonical Allele Identifier: CA1290821987
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135788077A= , CM000664.2:g.135788077A= GRCh38
NC_000002.11:g.136545647A= , CM000664.1:g.136545647A= GRCh37
NC_000002.10:g.136262117A= NCBI36
NG_008104.2:g.72093T= , LRG_338:g.72093T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.*247T= MANE Select ENSP00000264162.2:n.*247T=
ENST00000264162.6:c.*247T= ENSP00000264162.2:n.*247T=
NM_002299.2:c.*247T= , LRG_338t1:c.*247T= NP_002290.2:n.*247T=
NM_002299.3:c.*247T= NP_002290.2:n.*247T=
NM_002299.4:c.*247T= MANE Select NP_002290.2:n.*247T=