Canonical Allele Identifier: CA199285588
Gene: BRINP1 HGNC NCBI

Linked Data

dbSNP Id: rs917049403
MyVariant Identifiers: chr9:g.121984590A>G (hg19) chr9:g.119222312A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.119222312A>G , CM000671.2:g.119222312A>G GRCh38
NC_000009.11:g.121984590A>G , CM000671.1:g.121984590A>G GRCh37
NC_000009.10:g.121024411A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265922.8:c.686-8157T>C MANE Select ENSP00000265922.2:n.686-8157T>C
ENST00000265922.7:c.686-8157T>C ENSP00000265922.2:n.686-8157T>C
ENST00000373964.2:c.686-8157T>C ENSP00000363075.1:n.686-8157T>C
NM_014618.2:c.686-8157T>C NP_055433.2:n.686-8157T>C
NM_014618.3:c.686-8157T>C MANE Select NP_055433.2:n.686-8157T>C
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