Canonical Allele Identifier: CA335232860

Gene: GRIA3

Linked Data

• dbSNP Id: rs186465149
• gnomAD v2: X-122441688-C-T
• gnomAD v3: X-123307837-C-T
• gnomAD v4: X-123307837-C-T
• MyVariant Identifiers: chrX:g.122441688C>T (hg19) ; chrX:g.123307837C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123307837C>T , CM000685.2:g.123307837C>T	GRCh38
NC_000023.10:g.122441688C>T , CM000685.1:g.122441688C>T	GRCh37
NC_000023.9:g.122269369C>T	NCBI36
NG_009377.2:g.128595C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.509-18189C>T MANE Select	ENSP00000478489.1:n.509-18189C>T
ENST00000622768.5:c.509-18189C>T MANE Plus Clinical	ENSP00000481554.1:n.509-18189C>T
ENST00000541091.5:c.509-18189C>T	ENSP00000446440.2:n.509-18189C>T
ENST00000620443.1:c.509-18189C>T	ENSP00000478489.1:n.509-18189C>T
ENST00000620581.4:c.509-18189C>T	ENSP00000481875.1:n.509-18189C>T
ENST00000622768.4:c.509-18189C>T	ENSP00000481554.1:n.509-18189C>T
NM_000828.4:c.509-18189C>T	NP_000819.3:n.509-18189C>T
NM_007325.4:c.509-18189C>T	NP_015564.4:n.509-18189C>T
NM_007325.5:c.509-18189C>T MANE Select	NP_015564.5:n.509-18189C>T
NM_000828.5:c.509-18189C>T MANE Plus Clinical	NP_000819.4:n.509-18189C>T