Canonical Allele Identifier: CA1290826490
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135797991C= , CM000664.2:g.135797991C= GRCh38
NC_000002.11:g.136555561C= , CM000664.1:g.136555561C= GRCh37
NC_000002.10:g.136272031C= NCBI36
NG_008104.2:g.62179G= , LRG_338:g.62179G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4976+38G= MANE Select ENSP00000264162.2:n.4976+38G=
ENST00000264162.6:c.4976+38G= ENSP00000264162.2:n.4976+38G=
ENST00000452974.1:c.3069+38G= ENSP00000391231.1:n.3069+38G=
NM_002299.2:c.4976+38G= , LRG_338t1:c.4976+38G= NP_002290.2:n.4976+38G=
NM_002299.3:c.4976+38G= NP_002290.2:n.4976+38G=
XM_017004088.2:c.4976+38G= XP_016859577.1:n.4976+38G=
NM_002299.4:c.4976+38G= MANE Select NP_002290.2:n.4976+38G=