Canonical Allele Identifier: CA590173832

Gene: BRINP1

Linked Data

• dbSNP Id: rs1270577590
• gnomAD v2: 9-121984513-T-G
• gnomAD v3: 9-119222235-T-G
• gnomAD v4: 9-119222235-T-G
• MyVariant Identifiers: chr9:g.121984513T>G (hg19) ; chr9:g.119222235T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.119222235T>G , CM000671.2:g.119222235T>G	GRCh38
NC_000009.11:g.121984513T>G , CM000671.1:g.121984513T>G	GRCh37
NC_000009.10:g.121024334T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265922.8:c.686-8080A>C MANE Select	ENSP00000265922.2:n.686-8080A>C
ENST00000265922.7:c.686-8080A>C	ENSP00000265922.2:n.686-8080A>C
ENST00000373964.2:c.686-8080A>C	ENSP00000363075.1:n.686-8080A>C
NM_014618.2:c.686-8080A>C	NP_055433.2:n.686-8080A>C
NM_014618.3:c.686-8080A>C MANE Select	NP_055433.2:n.686-8080A>C