Canonical Allele Identifier: CA361050786
Gene: LECT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.135288647C>A (hg19) chr5:g.135952958C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952958C>A , CM000667.2:g.135952958C>A GRCh38
NC_000005.9:g.135288647C>A , CM000667.1:g.135288647C>A GRCh37
NC_000005.8:g.135316546C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274507.6:c.56G>T MANE Select ENSP00000274507.1:p.Gly19Val
ENST00000274507.5:c.56G>T ENSP00000274507.1:p.Gly19Val
ENST00000471827.1:n.159G>T
ENST00000512872.1:c.-161G>T ENSP00000427012.1:n.-161G>T
ENST00000514447.2:c.56G>T ENSP00000421123.2:p.Gly19Val
ENST00000522943.5:c.56G>T ENSP00000429618.1:p.Gly19Val
NM_002302.2:c.56G>T NP_002293.2:p.Gly19Val
NM_002302.3:c.56G>T MANE Select NP_002293.2:p.Gly19Val
Search 100 bp 5'
Search 100 bp 3'