Canonical Allele Identifier: CA470276958
Gene: NEUROG3 HGNC NCBI

Linked Data

dbSNP Id: rs1269114470
gnomAD v2: 10-71332206-G-A
gnomAD v4: 10-69572450-G-A
MyVariant Identifiers: chr10:g.71332206G>A (hg19) chr10:g.69572450G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69572450G>A , CM000672.2:g.69572450G>A GRCh38
NC_000010.10:g.71332206G>A , CM000672.1:g.71332206G>A GRCh37
NC_000010.9:g.71002212G>A NCBI36
NG_021321.1:g.6005C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242462.5:c.594C>T MANE Select ENSP00000242462.4:p.Thr198=
ENST00000242462.4:c.594C>T ENSP00000242462.4:p.Thr198=
NM_020999.3:c.594C>T NP_066279.2:p.Thr198=
XM_017016280.1:c.594C>T XP_016871769.1:p.Thr198=
NM_020999.4:c.594C>T MANE Select NP_066279.2:p.Thr198=
Search 100 bp 5'
Search 100 bp 3'