Canonical Allele Identifier: CA2661271314
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135788140-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135788140G>A , CM000664.2:g.135788140G>A GRCh38
NC_000002.11:g.136545710G>A , CM000664.1:g.136545710G>A GRCh37
NC_000002.10:g.136262180G>A NCBI36
NG_008104.2:g.72030C>T , LRG_338:g.72030C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*184C>T MANE Select ENSP00000264162.2:n.*184C>T
ENST00000264162.6:c.*184C>T ENSP00000264162.2:n.*184C>T
NM_002299.2:c.*184C>T , LRG_338t1:c.*184C>T NP_002290.2:n.*184C>T
NM_002299.3:c.*184C>T NP_002290.2:n.*184C>T
NM_002299.4:c.*184C>T MANE Select NP_002290.2:n.*184C>T
Search 100 bp 5'
Search 100 bp 3'