Canonical Allele Identifier: CA128075764
Gene: LECT2 HGNC NCBI

Linked Data

dbSNP Id: rs369985386
gnomAD v2: 5-135288560-C-G
gnomAD v3: 5-135952871-C-G
gnomAD v4: 5-135952871-C-G
MyVariant Identifiers: chr5:g.135288560C>G (hg19) chr5:g.135952871C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135952871C>G , CM000667.2:g.135952871C>G GRCh38
NC_000005.9:g.135288560C>G , CM000667.1:g.135288560C>G GRCh37
NC_000005.8:g.135316459C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274507.6:c.143G>C MANE Select ENSP00000274507.1:p.Arg48Thr
ENST00000274507.5:c.143G>C ENSP00000274507.1:p.Arg48Thr
ENST00000471827.1:n.246G>C
ENST00000512872.1:c.-74G>C ENSP00000427012.1:n.-74G>C
ENST00000514447.2:c.143G>C ENSP00000421123.2:p.Arg48Thr
ENST00000522943.5:c.143G>C ENSP00000429618.1:p.Arg48Thr
NM_002302.2:c.143G>C NP_002293.2:p.Arg48Thr
NM_002302.3:c.143G>C MANE Select NP_002293.2:p.Arg48Thr
Search 100 bp 5'
Search 100 bp 3'