Canonical Allele Identifier: CA3419876
Gene: LECT2 HGNC NCBI

Linked Data

dbSNP Id: rs769925563
ExAC: 5:135288654 G / A
gnomAD v2: 5-135288654-G-A
MyVariant Identifiers: chr5:g.135288654G>A (hg19) chr5:g.135952965G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952965G>A , CM000667.2:g.135952965G>A GRCh38
NC_000005.9:g.135288654G>A , CM000667.1:g.135288654G>A GRCh37
NC_000005.8:g.135316553G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274507.6:c.49C>T MANE Select ENSP00000274507.1:p.Leu17=
ENST00000274507.5:c.49C>T ENSP00000274507.1:p.Leu17=
ENST00000471827.1:n.152C>T
ENST00000512872.1:c.-168C>T ENSP00000427012.1:n.-168C>T
ENST00000514447.2:c.49C>T ENSP00000421123.2:p.Leu17=
ENST00000522943.5:c.49C>T ENSP00000429618.1:p.Leu17=
NM_002302.2:c.49C>T NP_002293.2:p.Leu17=
NM_002302.3:c.49C>T MANE Select NP_002293.2:p.Leu17=
Search 100 bp 5'
Search 100 bp 3'