Canonical Allele Identifier: CA2661274270
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135797892-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135797892G>T , CM000664.2:g.135797892G>T GRCh38
NC_000002.11:g.136555462G>T , CM000664.1:g.136555462G>T GRCh37
NC_000002.10:g.136271932G>T NCBI36
NG_008104.2:g.62278C>A , LRG_338:g.62278C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4976+137C>A MANE Select ENSP00000264162.2:n.4976+137C>A
ENST00000264162.6:c.4976+137C>A ENSP00000264162.2:n.4976+137C>A
ENST00000452974.1:c.3069+137C>A ENSP00000391231.1:n.3069+137C>A
NM_002299.2:c.4976+137C>A , LRG_338t1:c.4976+137C>A NP_002290.2:n.4976+137C>A
NM_002299.3:c.4976+137C>A NP_002290.2:n.4976+137C>A
XM_017004088.2:c.4976+137C>A XP_016859577.1:n.4976+137C>A
NM_002299.4:c.4976+137C>A MANE Select NP_002290.2:n.4976+137C>A
Search 100 bp 5'
Search 100 bp 3'