Canonical Allele Identifier: CA1128670085

Gene: BRINP1

Linked Data

• dbSNP Id: rs1830047142
• gnomAD v3: 9-119222149-A-G
• gnomAD v4: 9-119222149-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.119222149A>G , CM000671.2:g.119222149A>G	GRCh38
NC_000009.11:g.121984427A>G , CM000671.1:g.121984427A>G	GRCh37
NC_000009.10:g.121024248A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265922.8:c.686-7994T>C MANE Select	ENSP00000265922.2:n.686-7994T>C
ENST00000265922.7:c.686-7994T>C	ENSP00000265922.2:n.686-7994T>C
ENST00000373964.2:c.686-7994T>C	ENSP00000363075.1:n.686-7994T>C
NM_014618.2:c.686-7994T>C	NP_055433.2:n.686-7994T>C
NM_014618.3:c.686-7994T>C MANE Select	NP_055433.2:n.686-7994T>C