Canonical Allele Identifier: CA1884318132
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1832029020
gnomAD v4: 9-137139103-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139103G>T , CM000671.2:g.137139103G>T GRCh38
NC_000009.11:g.140033555G>T , CM000671.1:g.140033555G>T GRCh37
NC_000009.10:g.139153376G>T NCBI36
NG_011507.1:g.4947G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-384G>T ENSP00000360615.3:n.-384G>T
ENST00000371561.7:c.-384G>T ENSP00000360616.3:n.-384G>T
XM_005266073.4:c.-384G>T XP_005266130.1:n.-384G>T
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