Canonical Allele Identifier: CA478869503

Gene: GYS2

Linked Data

• dbSNP Id: rs1944273289
• MyVariant Identifiers: chr12:g.21715903T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21562969T>C , CM000674.2:g.21562969T>C	GRCh38
NC_000012.11:g.21715903T>C , CM000674.1:g.21715903T>C	GRCh37
NC_000012.10:g.21607170T>C	NCBI36
NG_016167.1:g.46879A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1011A>G MANE Select	ENSP00000261195.2:p.Lys337=
ENST00000647960.1:c.*1013A>G	ENSP00000497202.1:n.*1013A>G
ENST00000648372.1:n.938A>G
ENST00000261195.2:c.1011A>G	ENSP00000261195.2:p.Lys337=
NM_021957.3:c.1011A>G	NP_068776.2:p.Lys337=
XM_005253352.1:c.1011A>G	XP_005253409.1:p.Lys337=
XM_005253354.2:c.792A>G	XP_005253411.1:p.Lys264=
XM_006719062.2:c.1011A>G	XP_006719125.1:p.Lys337=
XM_006719063.2:c.780A>G	XP_006719126.1:p.Lys260=
NM_021957.4:c.1011A>G MANE Select	NP_068776.2:p.Lys337=
XM_006719063.3:c.780A>G	XP_006719126.1:p.Lys260=
XM_017019245.2:c.1011A>G	XP_016874734.1:p.Lys337=
XM_024448960.1:c.1011A>G	XP_024304728.1:p.Lys337=