Canonical Allele Identifier: CA895768539
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1304406247
MyVariant Identifiers: chr2:g.96916570T>C (hg19) chr2:g.96250832T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96250832T>C , CM000664.2:g.96250832T>C GRCh38
NC_000002.11:g.96916570T>C , CM000664.1:g.96916570T>C GRCh37
NC_000002.10:g.96280297T>C NCBI36
NG_027695.1:g.20182A>G , LRG_528:g.20182A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2976A>G MANE Select ENSP00000258439.3:n.*2976A>G
ENST00000258439.7:c.*2976A>G ENSP00000258439.2:n.*2976A>G
NM_001193304.2:c.*2976A>G NP_001180233.1:n.*2976A>G
NM_017849.3:c.*2976A>G , LRG_528t1:c.*2976A>G NP_060319.1:n.*2976A>G
XM_017004450.1:c.*2277A>G XP_016859939.1:n.*2277A>G
XM_017004452.1:c.*2976A>G XP_016859941.1:n.*2976A>G
NM_001193304.3:c.*2976A>G NP_001180233.1:n.*2976A>G
NM_017849.4:c.*2976A>G MANE Select NP_060319.1:n.*2976A>G
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