Canonical Allele Identifier: CA504884397
Gene: GRIN3B HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1004907C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004908C>G , CM000681.2:g.1004908C>G GRCh38
NC_000019.9:g.1004907C>G , CM000681.1:g.1004907C>G GRCh37
NC_000019.8:g.955907C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234389.3:c.1407C>G MANE Select ENSP00000234389.3:p.Pro469=
ENST00000588335.1:n.157C>G
NM_138690.1:c.1407C>G NP_619635.1:p.Pro469=
NM_138690.2:c.1407C>G NP_619635.1:p.Pro469=
XM_017026243.2:c.-172C>G XP_016881732.1:n.-172C>G
NM_138690.3:c.1407C>G MANE Select NP_619635.1:p.Pro469=
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