Canonical Allele Identifier: CA2148365869
Gene: TMED8 HGNC NCBI

Linked Data

dbSNP Id: rs1892832985
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77339093G>C , CM000676.2:g.77339093G>C GRCh38
NC_000014.8:g.77805436G>C , CM000676.1:g.77805436G>C GRCh37
NC_000014.7:g.76875189G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216468.8:c.*2678C>G MANE Select ENSP00000216468.7:n.*2678C>G
ENST00000216468.7:c.*2678C>G ENSP00000216468.7:n.*2678C>G
XM_005267544.3:c.*2678C>G XP_005267601.1:n.*2678C>G
NM_001346131.1:c.*2678C>G NP_001333060.1:n.*2678C>G
NM_001346133.1:c.*2678C>G NP_001333062.1:n.*2678C>G
NM_001346134.1:c.*2678C>G NP_001333063.1:n.*2678C>G
NM_213601.2:c.*2678C>G NP_998766.1:n.*2678C>G
XM_017021224.1:c.*2678C>G XP_016876713.1:n.*2678C>G
NM_213601.3:c.*2678C>G MANE Select NP_998766.1:n.*2678C>G
NM_001346131.2:c.*2678C>G NP_001333060.1:n.*2678C>G
NM_001346133.2:c.*2678C>G NP_001333062.1:n.*2678C>G
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