Canonical Allele Identifier: CA210633063
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs192800617
gnomAD v2: 10-87740794-C-A
gnomAD v3: 10-85981037-C-A
gnomAD v4: 10-85981037-C-A
MyVariant Identifiers: chr10:g.87740794C>A (hg19) chr10:g.85981037C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85981037C>A , CM000672.2:g.85981037C>A GRCh38
NC_000010.10:g.87740794C>A , CM000672.1:g.87740794C>A GRCh37
NC_000010.9:g.87730774C>A NCBI36
NG_011875.1:g.390457G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.727-64798G>T MANE Select ENSP00000330148.7:n.727-64798G>T
ENST00000327946.11:c.727-64798G>T ENSP00000330148.7:n.727-64798G>T
ENST00000464741.2:c.727-64798G>T ENSP00000433064.1:n.727-64798G>T
NM_017551.2:c.727-64798G>T NP_060021.1:n.727-64798G>T
XM_011539720.1:c.727-64798G>T XP_011538022.1:n.727-64798G>T
XM_011539720.2:c.727-64798G>T XP_011538022.1:n.727-64798G>T
NM_017551.3:c.727-64798G>T MANE Select NP_060021.1:n.727-64798G>T
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