Canonical Allele Identifier: CA1173014111
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1646576593

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135399C>T , CM000663.2:g.67135399C>T GRCh38
NC_000001.10:g.67601082C>T , CM000663.1:g.67601082C>T GRCh37
NC_000001.9:g.67373670C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371007.6:c.-103-4172G>A ENSP00000360046.1:n.-103-4172G>A
ENST00000448166.6:c.-103-4172G>A ENSP00000415519.2:n.-103-4172G>A
XM_011541466.1:c.-18+6215G>A XP_011539768.1:n.-18+6215G>A
XM_011541466.2:c.-18+6215G>A XP_011539768.1:n.-18+6215G>A