Canonical Allele Identifier: CA446550884
Gene: LECT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.135288649T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952960T>C , CM000667.2:g.135952960T>C GRCh38
NC_000005.9:g.135288649T>C , CM000667.1:g.135288649T>C GRCh37
NC_000005.8:g.135316548T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274507.6:c.54A>G MANE Select ENSP00000274507.1:p.Ala18=
ENST00000274507.5:c.54A>G ENSP00000274507.1:p.Ala18=
ENST00000471827.1:n.157A>G
ENST00000512872.1:c.-163A>G ENSP00000427012.1:n.-163A>G
ENST00000514447.2:c.54A>G ENSP00000421123.2:p.Ala18=
ENST00000522943.5:c.54A>G ENSP00000429618.1:p.Ala18=
NM_002302.2:c.54A>G NP_002293.2:p.Ala18=
NM_002302.3:c.54A>G MANE Select NP_002293.2:p.Ala18=
Search 100 bp 5'
Search 100 bp 3'