Canonical Allele Identifier: CA199285517
Gene: BRINP1 HGNC NCBI

Linked Data

dbSNP Id: rs904519359
gnomAD v3: 9-119222175-G-T
gnomAD v4: 9-119222175-G-T
MyVariant Identifiers: chr9:g.121984453G>T (hg19) chr9:g.119222175G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.119222175G>T , CM000671.2:g.119222175G>T GRCh38
NC_000009.11:g.121984453G>T , CM000671.1:g.121984453G>T GRCh37
NC_000009.10:g.121024274G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265922.8:c.686-8020C>A MANE Select ENSP00000265922.2:n.686-8020C>A
ENST00000265922.7:c.686-8020C>A ENSP00000265922.2:n.686-8020C>A
ENST00000373964.2:c.686-8020C>A ENSP00000363075.1:n.686-8020C>A
NM_014618.2:c.686-8020C>A NP_055433.2:n.686-8020C>A
NM_014618.3:c.686-8020C>A MANE Select NP_055433.2:n.686-8020C>A
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