Canonical Allele Identifier: CA2480159111
Gene: LCE1C HGNC NCBI

Linked Data

dbSNP Id: rs1652327134
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152805911A>C , CM000663.2:g.152805911A>C GRCh38
NC_000001.10:g.152778387A>C , CM000663.1:g.152778387A>C GRCh37
NC_000001.9:g.151045011A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607093.2:c.-20-413T>G MANE Select ENSP00000475270.1:n.-20-413T>G
ENST00000606576.1:c.-20-413T>G ENSP00000476034.1:n.-20-413T>G
NM_001276331.1:c.-20-413T>G NP_001263260.1:n.-20-413T>G
NM_178351.3:c.-20-413T>G NP_848128.1:n.-20-413T>G
NM_001276331.2:c.-20-413T>G NP_001263260.1:n.-20-413T>G
NM_178351.4:c.-20-413T>G MANE Select NP_848128.1:n.-20-413T>G
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