Canonical Allele Identifier: CA1036793074
Gene: LCT HGNC NCBI

Linked Data

gnomAD v3: 2-135788067-C-CG
gnomAD v4: 2-135788067-C-CG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135788067_135788068insG , CM000664.2:g.135788067_135788068insG GRCh38
NC_000002.11:g.136545637_136545638insG , CM000664.1:g.136545637_136545638insG GRCh37
NC_000002.10:g.136262107_136262108insG NCBI36
NG_008104.2:g.72102_72103insC , LRG_338:g.72102_72103insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*256_*257insC MANE Select ENSP00000264162.2:n.*256_*257insC
ENST00000264162.6:c.*256_*257insC ENSP00000264162.2:n.*256_*257insC
NM_002299.2:c.*256_*257insC , LRG_338t1:c.*256_*257insC NP_002290.2:n.*256_*257insC
NM_002299.3:c.*256_*257insC NP_002290.2:n.*256_*257insC
NM_002299.4:c.*256_*257insC MANE Select NP_002290.2:n.*256_*257insC
Search 100 bp 5'
Search 100 bp 3'