Canonical Allele Identifier: CA384132968

Gene: GYS2

Linked Data

• MyVariant Identifiers: chr12:g.21715940A>C (hg19) ; chr12:g.21563006A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21563006A>C , CM000674.2:g.21563006A>C	GRCh38
NC_000012.11:g.21715940A>C , CM000674.1:g.21715940A>C	GRCh37
NC_000012.10:g.21607207A>C	NCBI36
NG_016167.1:g.46842T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.974T>G MANE Select	ENSP00000261195.2:p.Phe325Cys
ENST00000647960.1:c.*976T>G	ENSP00000497202.1:n.*976T>G
ENST00000648372.1:n.901T>G
ENST00000261195.2:c.974T>G	ENSP00000261195.2:p.Phe325Cys
NM_021957.3:c.974T>G	NP_068776.2:p.Phe325Cys
XM_005253352.1:c.974T>G	XP_005253409.1:p.Phe325Cys
XM_005253354.2:c.755T>G	XP_005253411.1:p.Phe252Cys
XM_006719062.2:c.974T>G	XP_006719125.1:p.Phe325Cys
XM_006719063.2:c.743T>G	XP_006719126.1:p.Phe248Cys
NM_021957.4:c.974T>G MANE Select	NP_068776.2:p.Phe325Cys
XM_006719063.3:c.743T>G	XP_006719126.1:p.Phe248Cys
XM_017019245.2:c.974T>G	XP_016874734.1:p.Phe325Cys
XM_024448960.1:c.974T>G	XP_024304728.1:p.Phe325Cys