Canonical Allele Identifier: CA406697632
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs1970992635
gnomAD v3: 19-48419593-G-C
gnomAD v4: 19-48419593-G-C
MyVariant Identifiers: chr19:g.48922850G>C (hg19) chr19:g.48419593G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419593G>C , CM000681.2:g.48419593G>C GRCh38
NC_000019.9:g.48922850G>C , CM000681.1:g.48922850G>C GRCh37
NC_000019.8:g.53614662G>C NCBI36
NG_052829.1:g.29719G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1870G>C MANE Select ENSP00000263269.2:p.Gly624Arg
ENST00000263269.3:c.1870G>C ENSP00000263269.2:p.Gly624Arg
NM_000836.2:c.1870G>C NP_000827.2:p.Gly624Arg
XM_011526872.1:c.1870G>C XP_011525174.1:p.Gly624Arg
NM_000836.4:c.1870G>C MANE Select NP_000827.2:p.Gly624Arg
Search 100 bp 5'
Search 100 bp 3'