Canonical Allele Identifier: CA998565931
Gene: C1orf127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972940T>C , CM000663.2:g.10972940T>C GRCh38
NC_000001.10:g.11032997T>C , CM000663.1:g.11032997T>C GRCh37
NC_000001.9:g.10955584T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.8:n.128-2851A>G ENSP00000366203.4:n.128-2851A>G
ENST00000520253.1:n.61-2851A>G
NM_001170754.1:n.128-2851A>G NP_001164225.1:n.128-2851A>G
NM_001170754.2:c.128-2851A>G MANE Select NP_001164225.1:n.128-2851A>G