Canonical Allele Identifier: CA429093538

Gene: LCT

Linked Data

• MyVariant Identifiers: chr2:g.136590747A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833177A>G , CM000664.2:g.135833177A>G	GRCh38
NC_000002.11:g.136590747A>G , CM000664.1:g.136590747A>G	GRCh37
NC_000002.10:g.136307217A>G	NCBI36
NG_008104.2:g.26993T>C , LRG_338:g.26993T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264162.7:c.654T>C MANE Select	ENSP00000264162.2:p.Ser218=
ENST00000264162.6:c.654T>C	ENSP00000264162.2:p.Ser218=
NM_002299.2:c.654T>C , LRG_338t1:c.654T>C	NP_002290.2:p.Ser218=
NM_002299.3:c.654T>C	NP_002290.2:p.Ser218=
XM_017004088.2:c.654T>C	XP_016859577.1:p.Ser218=
NM_002299.4:c.654T>C MANE Select	NP_002290.2:p.Ser218=