Canonical Allele Identifier: CA30604079

Gene: LCE1C

Linked Data

• dbSNP Id: rs149410909
• gnomAD v2: 1-152778356-T-C
• gnomAD v3: 1-152805880-T-C
• gnomAD v4: 1-152805880-T-C
• MyVariant Identifiers: chr1:g.152778356T>C (hg19) ; chr1:g.152805880T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152805880T>C , CM000663.2:g.152805880T>C	GRCh38
NC_000001.10:g.152778356T>C , CM000663.1:g.152778356T>C	GRCh37
NC_000001.9:g.151044980T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607093.2:c.-20-382A>G MANE Select	ENSP00000475270.1:n.-20-382A>G
ENST00000606576.1:c.-20-382A>G	ENSP00000476034.1:n.-20-382A>G
NM_001276331.1:c.-20-382A>G	NP_001263260.1:n.-20-382A>G
NM_178351.3:c.-20-382A>G	NP_848128.1:n.-20-382A>G
NM_001276331.2:c.-20-382A>G	NP_001263260.1:n.-20-382A>G
NM_178351.4:c.-20-382A>G MANE Select	NP_848128.1:n.-20-382A>G