Canonical Allele Identifier: CA347656048
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014235
ClinVar RCV Id: RCV001312945
dbSNP Id: rs1684391872
gnomAD v4: 2-96265248-C-A
MyVariant Identifiers: chr2:g.96930986C>A (hg19) chr2:g.96265248C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265248C>A , CM000664.2:g.96265248C>A GRCh38
NC_000002.11:g.96930986C>A , CM000664.1:g.96930986C>A GRCh37
NC_000002.10:g.96294713C>A NCBI36
NG_027695.1:g.5766G>T , LRG_528:g.5766G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.134G>T MANE Select ENSP00000258439.3:p.Cys45Phe
ENST00000258439.7:c.134G>T ENSP00000258439.2:p.Cys45Phe
ENST00000432959.1:c.134G>T ENSP00000416660.1:p.Cys45Phe
NM_001193304.2:c.134G>T NP_001180233.1:p.Cys45Phe
NM_017849.3:c.134G>T , LRG_528t1:c.134G>T NP_060319.1:p.Cys45Phe
NM_001193304.3:c.134G>T NP_001180233.1:p.Cys45Phe
NM_017849.4:c.134G>T MANE Select NP_060319.1:p.Cys45Phe
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