Canonical Allele Identifier: CA368516610

Gene: GNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100677789A>C , CM000669.2:g.100677789A>C	GRCh38
NC_000007.13:g.100275412A>C , CM000669.1:g.100275412A>C	GRCh37
NC_000007.12:g.100113348A>C	NCBI36
NG_053106.1:g.21494T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005273.4:c.468A>C MANE Select	NP_005264.2:p.Gln156His
ENST00000303210.9:c.468A>C MANE Select	ENSP00000305260.4:p.Gln156His
NM_005273.3:c.468A>C	NP_005264.2:p.Gln156His
ENST00000303210.8:c.468A>C	ENSP00000305260.4:p.Gln156His
ENST00000393924.1:c.468A>C	ENSP00000377501.1:p.Gln156His
ENST00000393926.5:c.468A>C	ENSP00000377503.1:p.Gln156His
ENST00000419828.5:c.168A>C	ENSP00000390543.1:p.Gln56His
ENST00000424361.5:c.336A>C	ENSP00000389391.1:p.Gln112His
ENST00000427895.5:c.168A>C	ENSP00000400286.1:p.Gln56His
ENST00000431068.5:c.468A>C	ENSP00000390077.1:p.Gln156His
ENST00000436220.5:c.336A>C	ENSP00000401873.1:p.Gln112His
ENST00000451587.5:c.468A>C	ENSP00000399904.1:p.Gln156His
ENST00000469287.5:n.781A>C
ENST00000470354.1:n.338A>C