Canonical Allele Identifier: CA1153439937
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs1018739466
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972769C>A , CM000663.2:g.10972769C>A GRCh38
NC_000001.10:g.11032826C>A , CM000663.1:g.11032826C>A GRCh37
NC_000001.9:g.10955413C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.128-2680G>T MANE Select ENSP00000366203.4:n.128-2680G>T
ENST00000377004.8:c.128-2680G>T ENSP00000366203.4:n.128-2680G>T
ENST00000520253.1:c.61-2680G>T
NM_001170754.1:c.128-2680G>T NP_001164225.1:n.128-2680G>T
NM_001170754.2:c.128-2680G>T MANE Select NP_001164225.1:n.128-2680G>T
Search 100 bp 5'
Search 100 bp 3'