Canonical Allele Identifier: CA1173010270
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1646577793

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135500T>G , CM000663.2:g.67135500T>G GRCh38
NC_000001.10:g.67601183T>G , CM000663.1:g.67601183T>G GRCh37
NC_000001.9:g.67373771T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371007.6:c.-103-4273A>C ENSP00000360046.1:n.-103-4273A>C
ENST00000448166.6:c.-103-4273A>C ENSP00000415519.2:n.-103-4273A>C
XM_011541466.1:c.-18+6114A>C XP_011539768.1:n.-18+6114A>C
XM_011541466.2:c.-18+6114A>C XP_011539768.1:n.-18+6114A>C