Canonical Allele Identifier: CA376921423
Gene: NEUROG3 HGNC NCBI

Linked Data

dbSNP Id: rs1839225077
gnomAD v4: 10-69572457-C-T
MyVariant Identifiers: chr10:g.71332213C>T (hg19) chr10:g.69572457C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000242462.5:c.587G>A MANE Select ENSP00000242462.4:p.Gly196Glu
ENST00000242462.4:c.587G>A ENSP00000242462.4:p.Gly196Glu
NM_020999.3:c.587G>A NP_066279.2:p.Gly196Glu
XM_017016280.1:c.587G>A XP_016871769.1:p.Gly196Glu
NM_020999.4:c.587G>A MANE Select NP_066279.2:p.Gly196Glu
Search 100 bp 5'
Search 100 bp 3'