Canonical Allele Identifier: CA376921378
Gene: NEUROG3 HGNC NCBI

Linked Data

gnomAD v4: 10-69572451-G-T
MyVariant Identifiers: chr10:g.71332207G>T (hg19) chr10:g.69572451G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69572451G>T , CM000672.2:g.69572451G>T GRCh38
NC_000010.10:g.71332207G>T , CM000672.1:g.71332207G>T GRCh37
NC_000010.9:g.71002213G>T NCBI36
NG_021321.1:g.6004C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242462.5:c.593C>A MANE Select ENSP00000242462.4:p.Thr198Asn
ENST00000242462.4:c.593C>A ENSP00000242462.4:p.Thr198Asn
NM_020999.3:c.593C>A NP_066279.2:p.Thr198Asn
XM_017016280.1:c.593C>A XP_016871769.1:p.Thr198Asn
NM_020999.4:c.593C>A MANE Select NP_066279.2:p.Thr198Asn
Search 100 bp 5'
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