Canonical Allele Identifier: CA2021177027
Gene: GYS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21559399G= , CM000674.2:g.21559399G= GRCh38
NC_000012.11:g.21712333G= , CM000674.1:g.21712333G= GRCh37
NC_000012.10:g.21603600G= NCBI36
NG_016167.1:g.50449C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261195.3:c.1230-230C= MANE Select ENSP00000261195.2:n.1230-230C=
ENST00000647960.1:c.*1232-230C= ENSP00000497202.1:n.*1232-230C=
ENST00000648372.1:n.1157-230C=
ENST00000261195.2:c.1230-230C= ENSP00000261195.2:n.1230-230C=
NM_021957.3:c.1230-230C= NP_068776.2:n.1230-230C=
XM_005253352.1:c.1230-230C= XP_005253409.1:n.1230-230C=
XM_005253354.2:c.1011-230C= XP_005253411.1:n.1011-230C=
XM_006719062.2:c.1230-230C= XP_006719125.1:n.1230-230C=
XM_006719063.2:c.999-230C= XP_006719126.1:n.999-230C=
NM_021957.4:c.1230-230C= MANE Select NP_068776.2:n.1230-230C=
XM_006719063.3:c.999-230C= XP_006719126.1:n.999-230C=
XM_024448960.1:c.1230-230C= XP_024304728.1:n.1230-230C=