Canonical Allele Identifier: CA1173013980
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1558210761

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135206A>G , CM000663.2:g.67135206A>G GRCh38
NC_000001.10:g.67600889A>G , CM000663.1:g.67600889A>G GRCh37
NC_000001.9:g.67373477A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371007.6:c.-103-3979T>C ENSP00000360046.1:n.-103-3979T>C
ENST00000448166.6:c.-103-3979T>C ENSP00000415519.2:n.-103-3979T>C
XM_011541466.1:c.-18+6408T>C XP_011539768.1:n.-18+6408T>C
XM_011541466.2:c.-18+6408T>C XP_011539768.1:n.-18+6408T>C