Canonical Allele Identifier: CA408015344
Gene: TGM6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.2398094C>G (hg19) chr20:g.2417448C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2417448C>G , CM000682.2:g.2417448C>G GRCh38
NC_000020.10:g.2398094C>G , CM000682.1:g.2398094C>G GRCh37
NC_000020.9:g.2346094C>G NCBI36
NG_031917.1:g.41541C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000202625.7:c.1553C>G MANE Select ENSP00000202625.2:p.Ala518Gly
ENST00000202625.6:c.1553C>G ENSP00000202625.2:p.Ala518Gly
ENST00000381423.1:c.1553C>G ENSP00000370831.1:p.Ala518Gly
NM_001254734.1:c.1553C>G NP_001241663.1:p.Ala518Gly
NM_198994.2:c.1553C>G NP_945345.2:p.Ala518Gly
NM_001254734.2:c.1553C>G NP_001241663.1:p.Ala518Gly
NM_198994.3:c.1553C>G MANE Select NP_945345.2:p.Ala518Gly
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