Canonical Allele Identifier: CA9562995

Gene: GYS1

Linked Data

• dbSNP Id: rs763645797
• ExAC: 19:49478022 T / C
• gnomAD v2: 19-49478022-T-C
• gnomAD v3: 19-48974765-T-C
• gnomAD v4: 19-48974765-T-C
• MyVariant Identifiers: chr19:g.49478022T>C (hg19) ; chr19:g.48974765T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974765T>C , CM000681.2:g.48974765T>C	GRCh38
NC_000019.9:g.49478022T>C , CM000681.1:g.49478022T>C	GRCh37
NC_000019.8:g.54169834T>C	NCBI36
NG_012923.1:g.23589A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1309-32A>G MANE Select	ENSP00000317904.3:n.1309-32A>G
ENST00000263276.6:c.1117-32A>G	ENSP00000263276.6:n.1117-32A>G
ENST00000323798.7:c.1309-32A>G	ENSP00000317904.3:n.1309-32A>G
ENST00000472004.5:n.64-32A>G
ENST00000496048.1:n.216-32A>G
NM_001161587.1:c.1117-32A>G	NP_001155059.1:n.1117-32A>G
NM_002103.4:c.1309-32A>G	NP_002094.2:n.1309-32A>G
NR_027763.1:n.1368-32A>G
NM_002103.5:c.1309-32A>G MANE Select	NP_002094.2:n.1309-32A>G
NM_001161587.2:c.1117-32A>G	NP_001155059.1:n.1117-32A>G
NR_027763.2:n.1324-32A>G