Canonical Allele Identifier: CA440918096

Gene: BBS7

Linked Data

• MyVariant Identifiers: chr4:g.122749338T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121828183T>C , CM000666.2:g.121828183T>C	GRCh38
NC_000004.11:g.122749338T>C , CM000666.1:g.122749338T>C	GRCh37
NC_000004.10:g.122968788T>C	NCBI36
NG_009111.1:g.47305A>G
NG_052974.1:g.819A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264499.9:c.1977A>G MANE Select	ENSP00000264499.4:p.Glu659=
ENST00000264499.8:c.1977A>G	ENSP00000264499.4:p.Glu659=
ENST00000506636.1:c.1977A>G	ENSP00000423626.1:p.Glu659=
ENST00000507814.5:c.246A>G	ENSP00000423250.1:p.Glu82=
NM_018190.3:c.1977A>G	NP_060660.2:p.Glu659=
NM_176824.2:c.1977A>G	NP_789794.1:p.Glu659=
XM_005263106.2:c.1980A>G	XP_005263163.1:p.Glu660=
XM_011532079.1:c.2025A>G	XP_011530381.1:p.Glu675=
XM_011532080.1:c.2022A>G	XP_011530382.1:p.Glu674=
XM_011532081.1:c.1860A>G	XP_011530383.1:p.Glu620=
XM_005263106.4:c.1980A>G	XP_005263163.1:p.Glu660=
XM_011532079.3:c.2025A>G	XP_011530381.1:p.Glu675=
XM_011532080.3:c.2022A>G	XP_011530382.1:p.Glu674=
XM_011532081.3:c.1860A>G	XP_011530383.1:p.Glu620=
XM_017008357.2:c.1812A>G	XP_016863846.1:p.Glu604=
XM_017008358.2:c.1815A>G	XP_016863847.1:p.Glu605=
NM_176824.3:c.1977A>G MANE Select	NP_789794.1:p.Glu659=
NM_018190.4:c.1977A>G	NP_060660.2:p.Glu659=