Canonical Allele Identifier: CA427496285
Gene: TMEM127 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.96930907C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265169C>G , CM000664.2:g.96265169C>G GRCh38
NC_000002.11:g.96930907C>G , CM000664.1:g.96930907C>G GRCh37
NC_000002.10:g.96294634C>G NCBI36
NG_027695.1:g.5845G>C , LRG_528:g.5845G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.213G>C MANE Select ENSP00000258439.3:p.Val71=
ENST00000258439.7:c.213G>C ENSP00000258439.2:p.Val71=
ENST00000432959.1:c.213G>C ENSP00000416660.1:p.Val71=
NM_001193304.2:c.213G>C NP_001180233.1:p.Val71=
NM_017849.3:c.213G>C , LRG_528t1:c.213G>C NP_060319.1:p.Val71=
NM_001193304.3:c.213G>C NP_001180233.1:p.Val71=
NM_017849.4:c.213G>C MANE Select NP_060319.1:p.Val71=
Search 100 bp 5'
Search 100 bp 3'