Canonical Allele Identifier: CA429203323
Gene: LCT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.136564716T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135807146T>C , CM000664.2:g.135807146T>C GRCh38
NC_000002.11:g.136564716T>C , CM000664.1:g.136564716T>C GRCh37
NC_000002.10:g.136281186T>C NCBI36
NG_008104.2:g.53024A>G , LRG_338:g.53024A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4155A>G MANE Select ENSP00000264162.2:p.Ala1385=
ENST00000264162.6:c.4155A>G ENSP00000264162.2:p.Ala1385=
ENST00000452974.1:c.2451A>G ENSP00000391231.1:p.Ala817=
NM_002299.2:c.4155A>G , LRG_338t1:c.4155A>G NP_002290.2:p.Ala1385=
NM_002299.3:c.4155A>G NP_002290.2:p.Ala1385=
XM_017004088.2:c.4155A>G XP_016859577.1:p.Ala1385=
NM_002299.4:c.4155A>G MANE Select NP_002290.2:p.Ala1385=
Search 100 bp 5'
Search 100 bp 3'