Canonical Allele Identifier: CA429093519

Gene: LCT

Linked Data

• MyVariant Identifiers: chr2:g.136590723G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833153G>T , CM000664.2:g.135833153G>T	GRCh38
NC_000002.11:g.136590723G>T , CM000664.1:g.136590723G>T	GRCh37
NC_000002.10:g.136307193G>T	NCBI36
NG_008104.2:g.27017C>A , LRG_338:g.27017C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.678C>A MANE Select	ENSP00000264162.2:p.Ile226=
ENST00000264162.6:c.678C>A	ENSP00000264162.2:p.Ile226=
NM_002299.2:c.678C>A , LRG_338t1:c.678C>A	NP_002290.2:p.Ile226=
NM_002299.3:c.678C>A	NP_002290.2:p.Ile226=
XM_017004088.2:c.678C>A	XP_016859577.1:p.Ile226=
NM_002299.4:c.678C>A MANE Select	NP_002290.2:p.Ile226=