Canonical Allele Identifier: CA2661276694
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135833097-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135833097T>G , CM000664.2:g.135833097T>G GRCh38
NC_000002.11:g.136590667T>G , CM000664.1:g.136590667T>G GRCh37
NC_000002.10:g.136307137T>G NCBI36
NG_008104.2:g.27073A>C , LRG_338:g.27073A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.720+14A>C MANE Select ENSP00000264162.2:n.720+14A>C
ENST00000264162.6:c.720+14A>C ENSP00000264162.2:n.720+14A>C
NM_002299.2:c.720+14A>C , LRG_338t1:c.720+14A>C NP_002290.2:n.720+14A>C
NM_002299.3:c.720+14A>C NP_002290.2:n.720+14A>C
XM_017004088.2:c.720+14A>C XP_016859577.1:n.720+14A>C
NM_002299.4:c.720+14A>C MANE Select NP_002290.2:n.720+14A>C
Search 100 bp 5'
Search 100 bp 3'