Canonical Allele Identifier: CA446550882
Gene: LECT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.135288646C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952957C>G , CM000667.2:g.135952957C>G GRCh38
NC_000005.9:g.135288646C>G , CM000667.1:g.135288646C>G GRCh37
NC_000005.8:g.135316545C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274507.6:c.57G>C MANE Select ENSP00000274507.1:p.Gly19=
ENST00000274507.5:c.57G>C ENSP00000274507.1:p.Gly19=
ENST00000471827.1:n.160G>C
ENST00000512872.1:c.-160G>C ENSP00000427012.1:n.-160G>C
ENST00000514447.2:c.57G>C ENSP00000421123.2:p.Gly19=
ENST00000522943.5:c.57G>C ENSP00000429618.1:p.Gly19=
NM_002302.2:c.57G>C NP_002293.2:p.Gly19=
NM_002302.3:c.57G>C MANE Select NP_002293.2:p.Gly19=
Search 100 bp 5'
Search 100 bp 3'