Canonical Allele Identifier: CA1290821920
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs2077504370
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787914G>A , CM000664.2:g.135787914G>A GRCh38
NC_000002.11:g.136545484G>A , CM000664.1:g.136545484G>A GRCh37
NC_000002.10:g.136261954G>A NCBI36
NG_008104.2:g.72256C>T , LRG_338:g.72256C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*410C>T MANE Select ENSP00000264162.2:n.*410C>T
ENST00000264162.6:c.*410C>T ENSP00000264162.2:n.*410C>T
NM_002299.2:c.*410C>T , LRG_338t1:c.*410C>T NP_002290.2:n.*410C>T
NM_002299.3:c.*410C>T NP_002290.2:n.*410C>T
NM_002299.4:c.*410C>T MANE Select NP_002290.2:n.*410C>T
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