Canonical Allele Identifier: CA429085120
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs2077519404
gnomAD v3: 2-135789728-T-C
gnomAD v4: 2-135789728-T-C
MyVariant Identifiers: chr2:g.136547298T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789728T>C , CM000664.2:g.135789728T>C GRCh38
NC_000002.11:g.136547298T>C , CM000664.1:g.136547298T>C GRCh37
NC_000002.10:g.136263768T>C NCBI36
NG_008104.2:g.70442A>G , LRG_338:g.70442A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.5406A>G MANE Select ENSP00000264162.2:p.Thr1802=
ENST00000264162.6:c.5406A>G ENSP00000264162.2:p.Thr1802=
NM_002299.2:c.5406A>G , LRG_338t1:c.5406A>G NP_002290.2:p.Thr1802=
NM_002299.3:c.5406A>G NP_002290.2:p.Thr1802=
NM_002299.4:c.5406A>G MANE Select NP_002290.2:p.Thr1802=
Search 100 bp 5'
Search 100 bp 3'