Canonical Allele Identifier: CA1173014043
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1646575668
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135296G>A , CM000663.2:g.67135296G>A GRCh38
NC_000001.10:g.67600979G>A , CM000663.1:g.67600979G>A GRCh37
NC_000001.9:g.67373567G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371007.6:c.-103-4069C>T ENSP00000360046.1:n.-103-4069C>T
ENST00000448166.6:c.-103-4069C>T ENSP00000415519.2:n.-103-4069C>T
XM_011541466.1:c.-18+6318C>T XP_011539768.1:n.-18+6318C>T
XM_011541466.2:c.-18+6318C>T XP_011539768.1:n.-18+6318C>T
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