Canonical Allele Identifier: CA859394589

Gene: BRINP1

Linked Data

• dbSNP Id: rs1208202080
• MyVariant Identifiers: chr9:g.121984430G>A (hg19) ; chr9:g.119222152G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.119222152G>A , CM000671.2:g.119222152G>A	GRCh38
NC_000009.11:g.121984430G>A , CM000671.1:g.121984430G>A	GRCh37
NC_000009.10:g.121024251G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265922.8:c.686-7997C>T MANE Select	ENSP00000265922.2:n.686-7997C>T
ENST00000265922.7:c.686-7997C>T	ENSP00000265922.2:n.686-7997C>T
ENST00000373964.2:c.686-7997C>T	ENSP00000363075.1:n.686-7997C>T
NM_014618.2:c.686-7997C>T	NP_055433.2:n.686-7997C>T
NM_014618.3:c.686-7997C>T MANE Select	NP_055433.2:n.686-7997C>T