Canonical Allele Identifier: CA1153440184
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs1642976713

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10973139G>A , CM000663.2:g.10973139G>A GRCh38
NC_000001.10:g.11033196G>A , CM000663.1:g.11033196G>A GRCh37
NC_000001.9:g.10955783G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.127+3017C>T MANE Select ENSP00000366203.4:n.127+3017C>T
ENST00000377004.8:c.127+3017C>T ENSP00000366203.4:n.127+3017C>T
ENST00000520253.1:c.60+3017C>T
NM_001170754.1:c.127+3017C>T NP_001164225.1:n.127+3017C>T
NM_001170754.2:c.127+3017C>T MANE Select NP_001164225.1:n.127+3017C>T