Canonical Allele Identifier: CA348605825
Gene: LCT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.136575027C>A (hg19) chr2:g.135817457C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135817457C>A , CM000664.2:g.135817457C>A GRCh38
NC_000002.11:g.136575027C>A , CM000664.1:g.136575027C>A GRCh37
NC_000002.10:g.136291497C>A NCBI36
NG_008104.2:g.42713G>T , LRG_338:g.42713G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.1591G>T MANE Select ENSP00000264162.2:p.Gly531Trp
ENST00000264162.6:c.1591G>T ENSP00000264162.2:p.Gly531Trp
NM_002299.2:c.1591G>T , LRG_338t1:c.1591G>T NP_002290.2:p.Gly531Trp
NM_002299.3:c.1591G>T NP_002290.2:p.Gly531Trp
XM_017004088.2:c.1591G>T XP_016859577.1:p.Gly531Trp
NM_002299.4:c.1591G>T MANE Select NP_002290.2:p.Gly531Trp
Search 100 bp 5'
Search 100 bp 3'