Canonical Allele Identifier: CA52409542

Gene: TMEM127

Linked Data

• dbSNP Id: rs371926541
• gnomAD v3: 2-96250610-A-G
• gnomAD v4: 2-96250610-A-G
• MyVariant Identifiers: chr2:g.96916348A>G (hg19) ; chr2:g.96250610A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250610A>G , CM000664.2:g.96250610A>G	GRCh38
NC_000002.11:g.96916348A>G , CM000664.1:g.96916348A>G	GRCh37
NC_000002.10:g.96280075A>G	NCBI36
NG_027695.1:g.20404T>C , LRG_528:g.20404T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*3198T>C MANE Select	ENSP00000258439.3:n.*3198T>C
ENST00000258439.7:c.*3198T>C	ENSP00000258439.2:n.*3198T>C
NM_001193304.2:c.*3198T>C	NP_001180233.1:n.*3198T>C
NM_017849.3:c.*3198T>C , LRG_528t1:c.*3198T>C	NP_060319.1:n.*3198T>C
XM_017004450.1:c.*2499T>C	XP_016859939.1:n.*2499T>C
XM_017004452.1:c.*3198T>C	XP_016859941.1:n.*3198T>C
NM_001193304.3:c.*3198T>C	NP_001180233.1:n.*3198T>C
NM_017849.4:c.*3198T>C MANE Select	NP_060319.1:n.*3198T>C