Canonical Allele Identifier: CA12965832
Gene: GRIN3A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10121600

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615721C>T , CM000671.2:g.101615721C>T GRCh38
NC_000009.11:g.104378003C>T , CM000671.1:g.104378003C>T GRCh37
NC_000009.10:g.103417824C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_133445.2:c.2615-2194G>A VV NP_597702.2:p.=
XM_011518211.1:c.2615-2194G>A XP_011516513.1:p.=
XM_011518212.1:c.2615-2194G>A XP_011516514.1:p.=
XR_929711.1:n.2702-2194G>A
XM_011518211.2:c.2615-2194G>A XP_011516513.1:p.=
ENST00000361820.3:c.2615-2194G>A ENSP00000355155.3:p.=