Canonical Allele Identifier: CA376921416
Gene: NEUROG3 HGNC NCBI

Linked Data

gnomAD v4: 10-69572457-C-A
MyVariant Identifiers: chr10:g.71332213C>A (hg19) chr10:g.69572457C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69572457C>A , CM000672.2:g.69572457C>A GRCh38
NC_000010.10:g.71332213C>A , CM000672.1:g.71332213C>A GRCh37
NC_000010.9:g.71002219C>A NCBI36
NG_021321.1:g.5998G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242462.5:c.587G>T MANE Select ENSP00000242462.4:p.Gly196Val
ENST00000242462.4:c.587G>T ENSP00000242462.4:p.Gly196Val
NM_020999.3:c.587G>T NP_066279.2:p.Gly196Val
XM_017016280.1:c.587G>T XP_016871769.1:p.Gly196Val
NM_020999.4:c.587G>T MANE Select NP_066279.2:p.Gly196Val
Search 100 bp 5'
Search 100 bp 3'