Canonical Allele Identifier: CA478869525

Gene: GYS2

Linked Data

• MyVariant Identifiers: chr12:g.21715930A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21562996A>G , CM000674.2:g.21562996A>G	GRCh38
NC_000012.11:g.21715930A>G , CM000674.1:g.21715930A>G	GRCh37
NC_000012.10:g.21607197A>G	NCBI36
NG_016167.1:g.46852T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.984T>C MANE Select	ENSP00000261195.2:p.Ile328=
ENST00000647960.1:c.*986T>C	ENSP00000497202.1:n.*986T>C
ENST00000648372.1:n.911T>C
ENST00000261195.2:c.984T>C	ENSP00000261195.2:p.Ile328=
NM_021957.3:c.984T>C	NP_068776.2:p.Ile328=
XM_005253352.1:c.984T>C	XP_005253409.1:p.Ile328=
XM_005253354.2:c.765T>C	XP_005253411.1:p.Ile255=
XM_006719062.2:c.984T>C	XP_006719125.1:p.Ile328=
XM_006719063.2:c.753T>C	XP_006719126.1:p.Ile251=
NM_021957.4:c.984T>C MANE Select	NP_068776.2:p.Ile328=
XM_006719063.3:c.753T>C	XP_006719126.1:p.Ile251=
XM_017019245.2:c.984T>C	XP_016874734.1:p.Ile328=
XM_024448960.1:c.984T>C	XP_024304728.1:p.Ile328=