Canonical Allele Identifier: CA384122826

Gene: GYS2

Linked Data

• gnomAD v3: 12-21546467-T-A
• gnomAD v4: 12-21546467-T-A
• MyVariant Identifiers: chr12:g.21699401T>A (hg19) ; chr12:g.21546467T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21546467T>A , CM000674.2:g.21546467T>A	GRCh38
NC_000012.11:g.21699401T>A , CM000674.1:g.21699401T>A	GRCh37
NC_000012.10:g.21590668T>A	NCBI36
NG_016167.1:g.63381A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1426A>T MANE Select	ENSP00000261195.2:p.Ile476Phe
ENST00000647960.1:c.*1428A>T	ENSP00000497202.1:n.*1428A>T
ENST00000261195.2:c.1426A>T	ENSP00000261195.2:p.Ile476Phe
NM_021957.3:c.1426A>T	NP_068776.2:p.Ile476Phe
XM_005253352.1:c.1426A>T	XP_005253409.1:p.Ile476Phe
XM_005253354.2:c.1207A>T	XP_005253411.1:p.Ile403Phe
XM_006719062.2:c.1426A>T	XP_006719125.1:p.Ile476Phe
XM_006719063.2:c.1195A>T	XP_006719126.1:p.Ile399Phe
NM_021957.4:c.1426A>T MANE Select	NP_068776.2:p.Ile476Phe
XM_006719063.3:c.1195A>T	XP_006719126.1:p.Ile399Phe
XM_024448960.1:c.1426A>T	XP_024304728.1:p.Ile476Phe