Canonical Allele Identifier: CA2692773800
Gene: GRIN1 HGNC NCBI

Linked Data

gnomAD v4: 9-137139141-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139141T>C , CM000671.2:g.137139141T>C GRCh38
NC_000009.11:g.140033593T>C , CM000671.1:g.140033593T>C GRCh37
NC_000009.10:g.139153414T>C NCBI36
NG_011507.1:g.4985T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-346T>C ENSP00000360615.3:n.-346T>C
ENST00000371561.7:c.-346T>C ENSP00000360616.3:n.-346T>C
XM_005266073.3:c.-346T>C XP_005266130.1:n.-346T>C
XM_005266073.4:c.-346T>C XP_005266130.1:n.-346T>C
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