Canonical Allele Identifier: CA757423422
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs1426043930
MyVariant Identifiers: chr2:g.136555367A>T (hg19) chr2:g.135797797A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135797797A>T , CM000664.2:g.135797797A>T GRCh38
NC_000002.11:g.136555367A>T , CM000664.1:g.136555367A>T GRCh37
NC_000002.10:g.136271837A>T NCBI36
NG_008104.2:g.62373T>A , LRG_338:g.62373T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.4976+232T>A MANE Select ENSP00000264162.2:n.4976+232T>A
ENST00000264162.6:c.4976+232T>A ENSP00000264162.2:n.4976+232T>A
ENST00000452974.1:c.3069+232T>A ENSP00000391231.1:n.3069+232T>A
NM_002299.2:c.4976+232T>A , LRG_338t1:c.4976+232T>A NP_002290.2:n.4976+232T>A
NM_002299.3:c.4976+232T>A NP_002290.2:n.4976+232T>A
XM_017004088.2:c.4976+232T>A XP_016859577.1:n.4976+232T>A
NM_002299.4:c.4976+232T>A MANE Select NP_002290.2:n.4976+232T>A
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