Canonical Allele Identifier: CA885376192
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs1233935981
MyVariant Identifiers: chr1:g.11032880A>G (hg19) chr1:g.10972823A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972823A>G , CM000663.2:g.10972823A>G GRCh38
NC_000001.10:g.11032880A>G , CM000663.1:g.11032880A>G GRCh37
NC_000001.9:g.10955467A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.128-2734T>C MANE Select ENSP00000366203.4:n.128-2734T>C
ENST00000377004.8:c.128-2734T>C ENSP00000366203.4:n.128-2734T>C
ENST00000520253.1:c.61-2734T>C
NM_001170754.1:c.128-2734T>C NP_001164225.1:n.128-2734T>C
NM_001170754.2:c.128-2734T>C MANE Select NP_001164225.1:n.128-2734T>C
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