Canonical Allele Identifier: CA1876073058

Gene: BRINP1

Linked Data

• dbSNP Id: rs1830048407

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.119222286G>C , CM000671.2:g.119222286G>C	GRCh38
NC_000009.11:g.121984564G>C , CM000671.1:g.121984564G>C	GRCh37
NC_000009.10:g.121024385G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265922.8:c.686-8131C>G MANE Select	ENSP00000265922.2:n.686-8131C>G
ENST00000265922.7:c.686-8131C>G	ENSP00000265922.2:n.686-8131C>G
ENST00000373964.2:c.686-8131C>G	ENSP00000363075.1:n.686-8131C>G
NM_014618.2:c.686-8131C>G	NP_055433.2:n.686-8131C>G
NM_014618.3:c.686-8131C>G MANE Select	NP_055433.2:n.686-8131C>G