Canonical Allele Identifier: CA757423465
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs1214911970
MyVariant Identifiers: chr2:g.136555461del (hg19) chr2:g.135797891del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135797891del , CM000664.2:g.135797891del GRCh38
NC_000002.11:g.136555461del , CM000664.1:g.136555461del GRCh37
NC_000002.10:g.136271931del NCBI36
NG_008104.2:g.62279del , LRG_338:g.62279del

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4976+138del MANE Select ENSP00000264162.2:n.4976+138del
ENST00000264162.6:c.4976+138del ENSP00000264162.2:n.4976+138del
ENST00000452974.1:c.3069+138del ENSP00000391231.1:n.3069+138del
NM_002299.2:c.4976+138del , LRG_338t1:c.4976+138del NP_002290.2:n.4976+138del
NM_002299.3:c.4976+138del NP_002290.2:n.4976+138del
XM_017004088.2:c.4976+138del XP_016859577.1:n.4976+138del
NM_002299.4:c.4976+138del MANE Select NP_002290.2:n.4976+138del
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