Canonical Allele Identifier: CA358065937

Gene: BBS7

Linked Data

• MyVariant Identifiers: chr4:g.122775915A>T (hg19) ; chr4:g.121854760A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121854760A>T , CM000666.2:g.121854760A>T	GRCh38
NC_000004.11:g.122775915A>T , CM000666.1:g.122775915A>T	GRCh37
NC_000004.10:g.122995365A>T	NCBI36
NG_009111.1:g.20728T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264499.9:c.662T>A MANE Select	ENSP00000264499.4:p.Ile221Asn
ENST00000264499.8:c.662T>A	ENSP00000264499.4:p.Ile221Asn
ENST00000506636.1:c.662T>A	ENSP00000423626.1:p.Ile221Asn
NM_018190.3:c.662T>A	NP_060660.2:p.Ile221Asn
NM_176824.2:c.662T>A	NP_789794.1:p.Ile221Asn
XM_005263106.2:c.665T>A	XP_005263163.1:p.Ile222Asn
XM_011532079.1:c.710T>A	XP_011530381.1:p.Ile237Asn
XM_011532080.1:c.707T>A	XP_011530382.1:p.Ile236Asn
XM_011532081.1:c.710T>A	XP_011530383.1:p.Ile237Asn
XM_005263106.4:c.665T>A	XP_005263163.1:p.Ile222Asn
XM_011532079.3:c.710T>A	XP_011530381.1:p.Ile237Asn
XM_011532080.3:c.707T>A	XP_011530382.1:p.Ile236Asn
XM_011532081.3:c.710T>A	XP_011530383.1:p.Ile237Asn
XM_017008357.2:c.662T>A	XP_016863846.1:p.Ile221Asn
XM_017008358.2:c.665T>A	XP_016863847.1:p.Ile222Asn
NM_176824.3:c.662T>A MANE Select	NP_789794.1:p.Ile221Asn
NM_018190.4:c.662T>A	NP_060660.2:p.Ile221Asn