Canonical Allele Identifier: CA429093522

Gene: LCT

Linked Data

• MyVariant Identifiers: chr2:g.136590732A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833162A>C , CM000664.2:g.135833162A>C	GRCh38
NC_000002.11:g.136590732A>C , CM000664.1:g.136590732A>C	GRCh37
NC_000002.10:g.136307202A>C	NCBI36
NG_008104.2:g.27008T>G , LRG_338:g.27008T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.669T>G MANE Select	ENSP00000264162.2:p.Ala223=
ENST00000264162.6:c.669T>G	ENSP00000264162.2:p.Ala223=
NM_002299.2:c.669T>G , LRG_338t1:c.669T>G	NP_002290.2:p.Ala223=
NM_002299.3:c.669T>G	NP_002290.2:p.Ala223=
XM_017004088.2:c.669T>G	XP_016859577.1:p.Ala223=
NM_002299.4:c.669T>G MANE Select	NP_002290.2:p.Ala223=