Canonical Allele Identifier: CA2617923659

Gene: GYS2

Linked Data

• gnomAD v4: 12-21563124-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21563124G>A , CM000674.2:g.21563124G>A	GRCh38
NC_000012.11:g.21716058G>A , CM000674.1:g.21716058G>A	GRCh37
NC_000012.10:g.21607325G>A	NCBI36
NG_016167.1:g.46724C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.942-86C>T MANE Select	ENSP00000261195.2:n.942-86C>T
ENST00000647960.1:c.*944-86C>T	ENSP00000497202.1:n.*944-86C>T
ENST00000648372.1:n.869-86C>T
ENST00000261195.2:c.942-86C>T	ENSP00000261195.2:n.942-86C>T
NM_021957.3:c.942-86C>T	NP_068776.2:n.942-86C>T
XM_005253352.1:c.942-86C>T	XP_005253409.1:n.942-86C>T
XM_005253354.2:c.723-86C>T	XP_005253411.1:n.723-86C>T
XM_006719062.2:c.942-86C>T	XP_006719125.1:n.942-86C>T
XM_006719063.2:c.711-86C>T	XP_006719126.1:n.711-86C>T
NM_021957.4:c.942-86C>T MANE Select	NP_068776.2:n.942-86C>T
XM_006719063.3:c.711-86C>T	XP_006719126.1:n.711-86C>T
XM_017019245.2:c.942-86C>T	XP_016874734.1:n.942-86C>T
XM_024448960.1:c.942-86C>T	XP_024304728.1:n.942-86C>T