Canonical Allele Identifier: CA470276966
Gene: NEUROG3 HGNC NCBI

Linked Data

dbSNP Id: rs769211699
gnomAD v2: 10-71332209-G-A
MyVariant Identifiers: chr10:g.71332209G>A (hg19) chr10:g.69572453G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69572453G>A , CM000672.2:g.69572453G>A GRCh38
NC_000010.10:g.71332209G>A , CM000672.1:g.71332209G>A GRCh37
NC_000010.9:g.71002215G>A NCBI36
NG_021321.1:g.6002C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242462.5:c.591C>T MANE Select ENSP00000242462.4:p.Ala197=
ENST00000242462.4:c.591C>T ENSP00000242462.4:p.Ala197=
NM_020999.3:c.591C>T NP_066279.2:p.Ala197=
XM_017016280.1:c.591C>T XP_016871769.1:p.Ala197=
NM_020999.4:c.591C>T MANE Select NP_066279.2:p.Ala197=
Search 100 bp 5'
Search 100 bp 3'