Canonical Allele Identifier: CA427807841
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs2104283689
MyVariant Identifiers: chr2:g.96919669G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96253931G>A , CM000664.2:g.96253931G>A GRCh38
NC_000002.11:g.96919669G>A , CM000664.1:g.96919669G>A GRCh37
NC_000002.10:g.96283396G>A NCBI36
NG_027695.1:g.17083C>T , LRG_528:g.17083C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.594C>T MANE Select ENSP00000258439.3:p.His198=
ENST00000258439.7:c.594C>T ENSP00000258439.2:p.His198=
ENST00000432959.1:c.594C>T ENSP00000416660.1:p.His198=
ENST00000435268.1:c.342C>T ENSP00000411810.1:p.His114=
NM_001193304.2:c.594C>T NP_001180233.1:p.His198=
NM_017849.3:c.594C>T , LRG_528t1:c.594C>T NP_060319.1:p.His198=
XM_017004450.1:c.-325C>T XP_016859939.1:n.-325C>T
XM_017004452.1:c.342C>T XP_016859941.1:p.His114=
NM_001193304.3:c.594C>T NP_001180233.1:p.His198=
NM_017849.4:c.594C>T MANE Select NP_060319.1:p.His198=