Canonical Allele Identifier: CA2725947040

Gene: GYS2

Linked Data

• dbSNP Id: rs2136882717

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21563131G>A , CM000674.2:g.21563131G>A	GRCh38
NC_000012.11:g.21716065G>A , CM000674.1:g.21716065G>A	GRCh37
NC_000012.10:g.21607332G>A	NCBI36
NG_016167.1:g.46717C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.942-93C>T MANE Select	ENSP00000261195.2:n.942-93C>T
ENST00000647960.1:c.*944-93C>T	ENSP00000497202.1:n.*944-93C>T
ENST00000648372.1:n.869-93C>T
ENST00000261195.2:c.942-93C>T	ENSP00000261195.2:n.942-93C>T
NM_021957.3:c.942-93C>T	NP_068776.2:n.942-93C>T
XM_005253352.1:c.942-93C>T	XP_005253409.1:n.942-93C>T
XM_005253354.2:c.723-93C>T	XP_005253411.1:n.723-93C>T
XM_006719062.2:c.942-93C>T	XP_006719125.1:n.942-93C>T
XM_006719063.2:c.711-93C>T	XP_006719126.1:n.711-93C>T
NM_021957.4:c.942-93C>T MANE Select	NP_068776.2:n.942-93C>T
XM_006719063.3:c.711-93C>T	XP_006719126.1:n.711-93C>T
XM_017019245.2:c.942-93C>T	XP_016874734.1:n.942-93C>T
XM_024448960.1:c.942-93C>T	XP_024304728.1:n.942-93C>T