Canonical Allele Identifier: CA199553698
Gene: BRINP1 HGNC NCBI

Linked Data

dbSNP Id: rs1035448814
gnomAD v3: 9-119339310-G-A
gnomAD v4: 9-119339310-G-A
MyVariant Identifiers: chr9:g.122101588G>A (hg19) chr9:g.119339310G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.119339310G>A , CM000671.2:g.119339310G>A GRCh38
NC_000009.11:g.122101588G>A , CM000671.1:g.122101588G>A GRCh37
NC_000009.10:g.121141409G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265922.8:c.-50-25905C>T MANE Select ENSP00000265922.2:n.-50-25905C>T
ENST00000265922.7:c.-50-25905C>T ENSP00000265922.2:n.-50-25905C>T
ENST00000373964.2:c.-50-25905C>T ENSP00000363075.1:n.-50-25905C>T
NM_014618.2:c.-50-25905C>T NP_055433.2:n.-50-25905C>T
NM_014618.3:c.-50-25905C>T MANE Select NP_055433.2:n.-50-25905C>T
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