Canonical Allele Identifier: CA521155563
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs1369635933
gnomAD v2: 1-11032965-G-A
gnomAD v3: 1-10972908-G-A
gnomAD v4: 1-10972908-G-A
MyVariant Identifiers: chr1:g.11032965G>A (hg19) chr1:g.10972908G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972908G>A , CM000663.2:g.10972908G>A GRCh38
NC_000001.10:g.11032965G>A , CM000663.1:g.11032965G>A GRCh37
NC_000001.9:g.10955552G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377004.9:c.128-2819C>T MANE Select ENSP00000366203.4:n.128-2819C>T
ENST00000377004.8:c.128-2819C>T ENSP00000366203.4:n.128-2819C>T
ENST00000520253.1:c.61-2819C>T
NM_001170754.1:c.128-2819C>T NP_001164225.1:n.128-2819C>T
NM_001170754.2:c.128-2819C>T MANE Select NP_001164225.1:n.128-2819C>T
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