Canonical Allele Identifier: CA69727237
Gene: TMEM43 HGNC NCBI

Linked Data

dbSNP Id: rs1035579595
MyVariant Identifiers: chr3:g.14125115C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14125115C>G , CM000665.2:g.14125115C>G GRCh38
NC_000003.11:g.14166615C>G , CM000665.1:g.14166615C>G GRCh37
NC_000003.10:g.14141616C>G NCBI36
NG_008975.1:g.5176C>G , LRG_435:g.5176C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.-79C>G ENSP00000395617.1:n.-79C>G
ENST00000306077.5:c.-79C>G MANE Select ENSP00000303992.5:n.-79C>G
ENST00000306077.4:c.-79C>G ENSP00000303992.4:n.-79C>G
ENST00000432444.1:c.-79C>G ENSP00000395617.1:n.-79C>G
NM_024334.2:c.-79C>G , LRG_435t1:c.-79C>G NP_077310.1:n.-79C>G
XM_017007176.2:c.-415C>G XP_016862665.1:n.-415C>G
NM_024334.3:c.-79C>G MANE Select NP_077310.1:n.-79C>G
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