Canonical Allele Identifier: CA1173014087
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1646576349

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135381G>A , CM000663.2:g.67135381G>A GRCh38
NC_000001.10:g.67601064G>A , CM000663.1:g.67601064G>A GRCh37
NC_000001.9:g.67373652G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371007.6:c.-103-4154C>T ENSP00000360046.1:n.-103-4154C>T
ENST00000448166.6:c.-103-4154C>T ENSP00000415519.2:n.-103-4154C>T
XM_011541466.1:c.-18+6233C>T XP_011539768.1:n.-18+6233C>T
XM_011541466.2:c.-18+6233C>T XP_011539768.1:n.-18+6233C>T