Canonical Allele Identifier: CA2661275021
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135800926-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135800926C>A , CM000664.2:g.135800926C>A GRCh38
NC_000002.11:g.136558496C>A , CM000664.1:g.136558496C>A GRCh37
NC_000002.10:g.136274966C>A NCBI36
NG_008104.2:g.59244G>T , LRG_338:g.59244G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.4664-117G>T MANE Select ENSP00000264162.2:n.4664-117G>T
ENST00000264162.6:c.4664-117G>T ENSP00000264162.2:n.4664-117G>T
ENST00000452974.1:c.2960-2788G>T ENSP00000391231.1:n.2960-2788G>T
NM_002299.2:c.4664-117G>T , LRG_338t1:c.4664-117G>T NP_002290.2:n.4664-117G>T
NM_002299.3:c.4664-117G>T NP_002290.2:n.4664-117G>T
XM_017004088.2:c.4664-117G>T XP_016859577.1:n.4664-117G>T
NM_002299.4:c.4664-117G>T MANE Select NP_002290.2:n.4664-117G>T
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