Canonical Allele Identifier: CA199285520
Gene: BRINP1 HGNC NCBI

Linked Data

dbSNP Id: rs1000230785
MyVariant Identifiers: chr9:g.121984461T>C (hg19) chr9:g.119222183T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.119222183T>C , CM000671.2:g.119222183T>C GRCh38
NC_000009.11:g.121984461T>C , CM000671.1:g.121984461T>C GRCh37
NC_000009.10:g.121024282T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265922.8:c.686-8028A>G MANE Select ENSP00000265922.2:n.686-8028A>G
ENST00000265922.7:c.686-8028A>G ENSP00000265922.2:n.686-8028A>G
ENST00000373964.2:c.686-8028A>G ENSP00000363075.1:n.686-8028A>G
NM_014618.2:c.686-8028A>G NP_055433.2:n.686-8028A>G
NM_014618.3:c.686-8028A>G MANE Select NP_055433.2:n.686-8028A>G
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