Canonical Allele Identifier: CA376921347
Gene: NEUROG3 HGNC NCBI

Linked Data

gnomAD v4: 10-69572448-A-T
MyVariant Identifiers: chr10:g.71332204A>T (hg19) chr10:g.69572448A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69572448A>T , CM000672.2:g.69572448A>T GRCh38
NC_000010.10:g.71332204A>T , CM000672.1:g.71332204A>T GRCh37
NC_000010.9:g.71002210A>T NCBI36
NG_021321.1:g.6007T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000242462.5:c.596T>A MANE Select ENSP00000242462.4:p.Phe199Tyr
ENST00000242462.4:c.596T>A ENSP00000242462.4:p.Phe199Tyr
NM_020999.3:c.596T>A NP_066279.2:p.Phe199Tyr
XM_017016280.1:c.596T>A XP_016871769.1:p.Phe199Tyr
NM_020999.4:c.596T>A MANE Select NP_066279.2:p.Phe199Tyr
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