Canonical Allele Identifier: CA2692773763
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs2131184495
gnomAD v4: 9-137139113-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139113G>T , CM000671.2:g.137139113G>T GRCh38
NC_000009.11:g.140033565G>T , CM000671.1:g.140033565G>T GRCh37
NC_000009.10:g.139153386G>T NCBI36
NG_011507.1:g.4957G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-374G>T ENSP00000360615.3:n.-374G>T
ENST00000371561.7:c.-374G>T ENSP00000360616.3:n.-374G>T
XM_005266073.3:c.-374G>T XP_005266130.1:n.-374G>T
XM_005266073.4:c.-374G>T XP_005266130.1:n.-374G>T
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