Canonical Allele Identifier: CA427496396
Gene: TMEM127 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.96931027C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265289C>G , CM000664.2:g.96265289C>G GRCh38
NC_000002.11:g.96931027C>G , CM000664.1:g.96931027C>G GRCh37
NC_000002.10:g.96294754C>G NCBI36
NG_027695.1:g.5725G>C , LRG_528:g.5725G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.93G>C MANE Select ENSP00000258439.3:p.Leu31=
ENST00000258439.7:c.93G>C ENSP00000258439.2:p.Leu31=
ENST00000432959.1:c.93G>C ENSP00000416660.1:p.Leu31=
NM_001193304.2:c.93G>C NP_001180233.1:p.Leu31=
NM_017849.3:c.93G>C , LRG_528t1:c.93G>C NP_060319.1:p.Leu31=
NM_001193304.3:c.93G>C NP_001180233.1:p.Leu31=
NM_017849.4:c.93G>C MANE Select NP_060319.1:p.Leu31=
Search 100 bp 5'
Search 100 bp 3'