Canonical Allele Identifier: CA1033956974
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1684071737
gnomAD v3: 2-96250798-T-C
gnomAD v4: 2-96250798-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96250798T>C , CM000664.2:g.96250798T>C GRCh38
NC_000002.11:g.96916536T>C , CM000664.1:g.96916536T>C GRCh37
NC_000002.10:g.96280263T>C NCBI36
NG_027695.1:g.20216A>G , LRG_528:g.20216A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*3010A>G MANE Select ENSP00000258439.3:n.*3010A>G
ENST00000258439.7:c.*3010A>G ENSP00000258439.2:n.*3010A>G
NM_001193304.2:c.*3010A>G NP_001180233.1:n.*3010A>G
NM_017849.3:c.*3010A>G , LRG_528t1:c.*3010A>G NP_060319.1:n.*3010A>G
XM_017004450.1:c.*2311A>G XP_016859939.1:n.*2311A>G
XM_017004452.1:c.*3010A>G XP_016859941.1:n.*3010A>G
NM_001193304.3:c.*3010A>G NP_001180233.1:n.*3010A>G
NM_017849.4:c.*3010A>G MANE Select NP_060319.1:n.*3010A>G
Search 100 bp 5'
Search 100 bp 3'