Canonical Allele Identifier: CA2480159142
Gene: LCE1C HGNC NCBI

Linked Data

dbSNP Id: rs1652329096
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152805976G>A , CM000663.2:g.152805976G>A GRCh38
NC_000001.10:g.152778452G>A , CM000663.1:g.152778452G>A GRCh37
NC_000001.9:g.151045076G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000607093.2:c.-20-478C>T MANE Select ENSP00000475270.1:n.-20-478C>T
ENST00000606576.1:c.-20-478C>T ENSP00000476034.1:n.-20-478C>T
NM_001276331.1:c.-20-478C>T NP_001263260.1:n.-20-478C>T
NM_178351.3:c.-20-478C>T NP_848128.1:n.-20-478C>T
NM_001276331.2:c.-20-478C>T NP_001263260.1:n.-20-478C>T
NM_178351.4:c.-20-478C>T MANE Select NP_848128.1:n.-20-478C>T
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