Canonical Allele Identifier: CA738098902
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1386512852
gnomAD v3: 1-67135532-A-G
gnomAD v4: 1-67135532-A-G
MyVariant Identifiers: chr1:g.67601215A>G (hg19) chr1:g.67135532A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135532A>G , CM000663.2:g.67135532A>G GRCh38
NC_000001.10:g.67601215A>G , CM000663.1:g.67601215A>G GRCh37
NC_000001.9:g.67373803A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371007.6:c.-103-4305T>C ENSP00000360046.1:n.-103-4305T>C
ENST00000448166.6:c.-103-4305T>C ENSP00000415519.2:n.-103-4305T>C
XM_011541466.1:c.-18+6082T>C XP_011539768.1:n.-18+6082T>C
XM_011541466.2:c.-18+6082T>C XP_011539768.1:n.-18+6082T>C
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