Canonical Allele Identifier: CA429204538
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs2077789248
MyVariant Identifiers: chr2:g.136575031T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135817461T>A , CM000664.2:g.135817461T>A GRCh38
NC_000002.11:g.136575031T>A , CM000664.1:g.136575031T>A GRCh37
NC_000002.10:g.136291501T>A NCBI36
NG_008104.2:g.42709A>T , LRG_338:g.42709A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.1587A>T MANE Select ENSP00000264162.2:p.Thr529=
ENST00000264162.6:c.1587A>T ENSP00000264162.2:p.Thr529=
NM_002299.2:c.1587A>T , LRG_338t1:c.1587A>T NP_002290.2:p.Thr529=
NM_002299.3:c.1587A>T NP_002290.2:p.Thr529=
XM_017004088.2:c.1587A>T XP_016859577.1:p.Thr529=
NM_002299.4:c.1587A>T MANE Select NP_002290.2:p.Thr529=
Search 100 bp 5'
Search 100 bp 3'