Canonical Allele Identifier: CA1127422784
Gene: GRIN3A HGNC NCBI

Linked Data

gnomAD v3: 9-101615631-A-T
gnomAD v4: 9-101615631-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615631A>T , CM000671.2:g.101615631A>T GRCh38
NC_000009.11:g.104377913A>T , CM000671.1:g.104377913A>T GRCh37
NC_000009.10:g.103417734A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2615-2104T>A MANE Select ENSP00000355155.3:n.2615-2104T>A
ENST00000361820.3:c.2615-2104T>A ENSP00000355155.3:n.2615-2104T>A
NM_133445.2:c.2615-2104T>A NP_597702.2:n.2615-2104T>A
XM_011518211.1:c.2615-2104T>A XP_011516513.1:n.2615-2104T>A
XM_011518212.1:c.2615-2104T>A XP_011516514.1:n.2615-2104T>A
XR_929711.1:n.2702-2104T>A
XM_011518211.2:c.2615-2104T>A XP_011516513.1:n.2615-2104T>A
NM_133445.3:c.2615-2104T>A MANE Select NP_597702.2:n.2615-2104T>A
Search 100 bp 5'
Search 100 bp 3'