Canonical Allele Identifier: CA10762984
Gene: C1orf127 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12565727

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10973025A>G , CM000663.2:g.10973025A>G GRCh38
NC_000001.10:g.11033082A>G , CM000663.1:g.11033082A>G GRCh37
NC_000001.9:g.10955669A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001170754.1:n.128-2936T>C VV NP_001164225.1:p.=
ENST00000377004.8:n.128-2936T>C ENSP00000366203.4:p.=
ENST00000520253.1:n.61-2936T>C