Canonical Allele Identifier: CA2661275105
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135807076-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135807076G>A , CM000664.2:g.135807076G>A GRCh38
NC_000002.11:g.136564646G>A , CM000664.1:g.136564646G>A GRCh37
NC_000002.10:g.136281116G>A NCBI36
NG_008104.2:g.53094C>T , LRG_338:g.53094C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4173+52C>T MANE Select ENSP00000264162.2:n.4173+52C>T
ENST00000264162.6:c.4173+52C>T ENSP00000264162.2:n.4173+52C>T
ENST00000452974.1:c.2469+52C>T ENSP00000391231.1:n.2469+52C>T
NM_002299.2:c.4173+52C>T , LRG_338t1:c.4173+52C>T NP_002290.2:n.4173+52C>T
NM_002299.3:c.4173+52C>T NP_002290.2:n.4173+52C>T
XM_017004088.2:c.4173+52C>T XP_016859577.1:n.4173+52C>T
NM_002299.4:c.4173+52C>T MANE Select NP_002290.2:n.4173+52C>T
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