Canonical Allele Identifier: CA446550888
Gene: LECT2 HGNC NCBI

Linked Data

dbSNP Id: rs1763815780
gnomAD v4: 5-135952963-C-T
MyVariant Identifiers: chr5:g.135288652C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952963C>T , CM000667.2:g.135952963C>T GRCh38
NC_000005.9:g.135288652C>T , CM000667.1:g.135288652C>T GRCh37
NC_000005.8:g.135316551C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274507.6:c.51G>A MANE Select ENSP00000274507.1:p.Leu17=
ENST00000274507.5:c.51G>A ENSP00000274507.1:p.Leu17=
ENST00000471827.1:n.154G>A
ENST00000512872.1:c.-166G>A ENSP00000427012.1:n.-166G>A
ENST00000514447.2:c.51G>A ENSP00000421123.2:p.Leu17=
ENST00000522943.5:c.51G>A ENSP00000429618.1:p.Leu17=
NM_002302.2:c.51G>A NP_002293.2:p.Leu17=
NM_002302.3:c.51G>A MANE Select NP_002293.2:p.Leu17=
Search 100 bp 5'
Search 100 bp 3'