Canonical Allele Identifier: CA197314528
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs981871769
MyVariant Identifiers: chr9:g.104377912C>T (hg19) chr9:g.101615630C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615630C>T , CM000671.2:g.101615630C>T GRCh38
NC_000009.11:g.104377912C>T , CM000671.1:g.104377912C>T GRCh37
NC_000009.10:g.103417733C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2615-2103G>A MANE Select ENSP00000355155.3:n.2615-2103G>A
ENST00000361820.3:c.2615-2103G>A ENSP00000355155.3:n.2615-2103G>A
NM_133445.2:c.2615-2103G>A NP_597702.2:n.2615-2103G>A
XM_011518211.1:c.2615-2103G>A XP_011516513.1:n.2615-2103G>A
XM_011518212.1:c.2615-2103G>A XP_011516514.1:n.2615-2103G>A
XR_929711.1:n.2702-2103G>A
XM_011518211.2:c.2615-2103G>A XP_011516513.1:n.2615-2103G>A
NM_133445.3:c.2615-2103G>A MANE Select NP_597702.2:n.2615-2103G>A
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