Canonical Allele Identifier: CA1290821986
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs2077505588
gnomAD v4: 2-135788075-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135788075A>T , CM000664.2:g.135788075A>T GRCh38
NC_000002.11:g.136545645A>T , CM000664.1:g.136545645A>T GRCh37
NC_000002.10:g.136262115A>T NCBI36
NG_008104.2:g.72095T>A , LRG_338:g.72095T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.*249T>A MANE Select ENSP00000264162.2:n.*249T>A
ENST00000264162.6:c.*249T>A ENSP00000264162.2:n.*249T>A
NM_002299.2:c.*249T>A , LRG_338t1:c.*249T>A NP_002290.2:n.*249T>A
NM_002299.3:c.*249T>A NP_002290.2:n.*249T>A
NM_002299.4:c.*249T>A MANE Select NP_002290.2:n.*249T>A
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