Canonical Allele Identifier: CA895769429
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1382471948
MyVariant Identifiers: chr2:g.96918179A>G (hg19) chr2:g.96252441A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96252441A>G , CM000664.2:g.96252441A>G GRCh38
NC_000002.11:g.96918179A>G , CM000664.1:g.96918179A>G GRCh37
NC_000002.10:g.96281906A>G NCBI36
NG_027695.1:g.18573T>C , LRG_528:g.18573T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*1367T>C MANE Select ENSP00000258439.3:n.*1367T>C
ENST00000258439.7:c.*1367T>C ENSP00000258439.2:n.*1367T>C
ENST00000432959.1:c.*1367T>C ENSP00000416660.1:n.*1367T>C
NM_001193304.2:c.*1367T>C NP_001180233.1:n.*1367T>C
NM_017849.3:c.*1367T>C , LRG_528t1:c.*1367T>C NP_060319.1:n.*1367T>C
XM_017004450.1:c.*668T>C XP_016859939.1:n.*668T>C
XM_017004452.1:c.*1367T>C XP_016859941.1:n.*1367T>C
NM_001193304.3:c.*1367T>C NP_001180233.1:n.*1367T>C
NM_017849.4:c.*1367T>C MANE Select NP_060319.1:n.*1367T>C
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