Canonical Allele Identifier: CA23513378
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1018130664
gnomAD v2: 1-67601073-T-C
gnomAD v3: 1-67135390-T-C
gnomAD v4: 1-67135390-T-C
MyVariant Identifiers: chr1:g.67601073T>C (hg19) chr1:g.67135390T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135390T>C , CM000663.2:g.67135390T>C GRCh38
NC_000001.10:g.67601073T>C , CM000663.1:g.67601073T>C GRCh37
NC_000001.9:g.67373661T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371007.6:c.-103-4163A>G ENSP00000360046.1:n.-103-4163A>G
ENST00000448166.6:c.-103-4163A>G ENSP00000415519.2:n.-103-4163A>G
XM_011541466.1:c.-18+6224A>G XP_011539768.1:n.-18+6224A>G
XM_011541466.2:c.-18+6224A>G XP_011539768.1:n.-18+6224A>G
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