Canonical Allele Identifier: CA895725267
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1410646371
MyVariant Identifiers: chr2:g.96931625G>C (hg19) chr2:g.96265887G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265887G>C , CM000664.2:g.96265887G>C GRCh38
NC_000002.11:g.96931625G>C , CM000664.1:g.96931625G>C GRCh37
NC_000002.10:g.96295352G>C NCBI36
NG_027695.1:g.5127C>G , LRG_528:g.5127C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.-150C>G MANE Select ENSP00000258439.3:n.-150C>G
ENST00000258439.7:c.-150C>G ENSP00000258439.2:n.-150C>G
ENST00000432959.1:c.-127C>G ENSP00000416660.1:n.-127C>G
NM_001193304.2:c.-127C>G NP_001180233.1:n.-127C>G
NM_017849.3:c.-150C>G , LRG_528t1:c.-150C>G NP_060319.1:n.-150C>G
NM_001193304.3:c.-127C>G NP_001180233.1:n.-127C>G
NM_017849.4:c.-150C>G MANE Select NP_060319.1:n.-150C>G
Search 100 bp 5'
Search 100 bp 3'