Canonical Allele Identifier: CA2661271092
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135787902-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787902A>C , CM000664.2:g.135787902A>C GRCh38
NC_000002.11:g.136545472A>C , CM000664.1:g.136545472A>C GRCh37
NC_000002.10:g.136261942A>C NCBI36
NG_008104.2:g.72268T>G , LRG_338:g.72268T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*422T>G MANE Select ENSP00000264162.2:n.*422T>G
ENST00000264162.6:c.*422T>G ENSP00000264162.2:n.*422T>G
NM_002299.2:c.*422T>G , LRG_338t1:c.*422T>G NP_002290.2:n.*422T>G
NM_002299.3:c.*422T>G NP_002290.2:n.*422T>G
NM_002299.4:c.*422T>G MANE Select NP_002290.2:n.*422T>G
Search 100 bp 5'
Search 100 bp 3'