Canonical Allele Identifier: CA9562997

Gene: GYS1

Linked Data

• dbSNP Id: rs761667733
• ExAC: 19:49478029 G / A
• gnomAD v2: 19-49478029-G-A
• gnomAD v3: 19-48974772-G-A
• gnomAD v4: 19-48974772-G-A
• MyVariant Identifiers: chr19:g.49478029G>A (hg19) ; chr19:g.48974772G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48974772G>A , CM000681.2:g.48974772G>A	GRCh38
NC_000019.9:g.49478029G>A , CM000681.1:g.49478029G>A	GRCh37
NC_000019.8:g.54169841G>A	NCBI36
NG_012923.1:g.23582C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323798.8:c.1309-39C>T MANE Select	ENSP00000317904.3:n.1309-39C>T
ENST00000263276.6:c.1117-39C>T	ENSP00000263276.6:n.1117-39C>T
ENST00000323798.7:c.1309-39C>T	ENSP00000317904.3:n.1309-39C>T
ENST00000472004.5:n.64-39C>T
ENST00000496048.1:n.216-39C>T
NM_001161587.1:c.1117-39C>T	NP_001155059.1:n.1117-39C>T
NM_002103.4:c.1309-39C>T	NP_002094.2:n.1309-39C>T
NR_027763.1:n.1368-39C>T
NM_002103.5:c.1309-39C>T MANE Select	NP_002094.2:n.1309-39C>T
NM_001161587.2:c.1117-39C>T	NP_001155059.1:n.1117-39C>T
NR_027763.2:n.1324-39C>T