Canonical Allele Identifier: CA1153440026
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs1045899545

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972916C>T , CM000663.2:g.10972916C>T GRCh38
NC_000001.10:g.11032973C>T , CM000663.1:g.11032973C>T GRCh37
NC_000001.9:g.10955560C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.128-2827G>A MANE Select ENSP00000366203.4:n.128-2827G>A
ENST00000377004.8:c.128-2827G>A ENSP00000366203.4:n.128-2827G>A
ENST00000520253.1:c.61-2827G>A
NM_001170754.1:c.128-2827G>A NP_001164225.1:n.128-2827G>A
NM_001170754.2:c.128-2827G>A MANE Select NP_001164225.1:n.128-2827G>A