Canonical Allele Identifier: CA738098822
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1374331114
gnomAD v3: 1-67135379-A-C
gnomAD v4: 1-67135379-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135379A>C , CM000663.2:g.67135379A>C GRCh38
NC_000001.10:g.67601062A>C , CM000663.1:g.67601062A>C GRCh37
NC_000001.9:g.67373650A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371007.6:c.-103-4152T>G ENSP00000360046.1:n.-103-4152T>G
ENST00000448166.6:c.-103-4152T>G ENSP00000415519.2:n.-103-4152T>G
XM_011541466.1:c.-18+6235T>G XP_011539768.1:n.-18+6235T>G
XM_011541466.2:c.-18+6235T>G XP_011539768.1:n.-18+6235T>G