Canonical Allele Identifier: CA429086395

Gene: LCT

Linked Data

• MyVariant Identifiers: chr2:g.136558264C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135800694C>G , CM000664.2:g.135800694C>G	GRCh38
NC_000002.11:g.136558264C>G , CM000664.1:g.136558264C>G	GRCh37
NC_000002.10:g.136274734C>G	NCBI36
NG_008104.2:g.59476G>C , LRG_338:g.59476G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4779G>C MANE Select	ENSP00000264162.2:p.Val1593=
ENST00000264162.6:c.4779G>C	ENSP00000264162.2:p.Val1593=
ENST00000452974.1:c.2960-2556G>C	ENSP00000391231.1:n.2960-2556G>C
NM_002299.2:c.4779G>C , LRG_338t1:c.4779G>C	NP_002290.2:p.Val1593=
NM_002299.3:c.4779G>C	NP_002290.2:p.Val1593=
XM_017004088.2:c.4779G>C	XP_016859577.1:p.Val1593=
NM_002299.4:c.4779G>C MANE Select	NP_002290.2:p.Val1593=