Canonical Allele Identifier: CA2660177924
Gene: TMEM127 HGNC NCBI

Linked Data

gnomAD v4: 2-96265901-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265901G>A , CM000664.2:g.96265901G>A GRCh38
NC_000002.11:g.96931639G>A , CM000664.1:g.96931639G>A GRCh37
NC_000002.10:g.96295366G>A NCBI36
NG_027695.1:g.5113C>T , LRG_528:g.5113C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.-164C>T MANE Select ENSP00000258439.3:n.-164C>T
ENST00000258439.7:c.-164C>T ENSP00000258439.2:n.-164C>T
ENST00000432959.1:c.-141C>T ENSP00000416660.1:n.-141C>T
NM_001193304.2:c.-141C>T NP_001180233.1:n.-141C>T
NM_017849.3:c.-164C>T , LRG_528t1:c.-164C>T NP_060319.1:n.-164C>T
NM_001193304.3:c.-141C>T NP_001180233.1:n.-141C>T
NM_017849.4:c.-164C>T MANE Select NP_060319.1:n.-164C>T
Search 100 bp 5'
Search 100 bp 3'