Canonical Allele Identifier: CA2575098327
Gene: GYS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21546485T>G , CM000674.2:g.21546485T>G GRCh38
NC_000012.11:g.21699419T>G , CM000674.1:g.21699419T>G GRCh37
NC_000012.10:g.21590686T>G NCBI36
NG_016167.1:g.63363A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261195.3:c.1423-15A>C MANE Select ENSP00000261195.2:n.1423-15A>C
ENST00000647960.1:c.*1425-15A>C ENSP00000497202.1:n.*1425-15A>C
ENST00000261195.2:c.1423-15A>C ENSP00000261195.2:n.1423-15A>C
NM_021957.3:c.1423-15A>C NP_068776.2:n.1423-15A>C
XM_005253352.1:c.1423-15A>C XP_005253409.1:n.1423-15A>C
XM_005253354.2:c.1204-15A>C XP_005253411.1:n.1204-15A>C
XM_006719062.2:c.1423-15A>C XP_006719125.1:n.1423-15A>C
XM_006719063.2:c.1192-15A>C XP_006719126.1:n.1192-15A>C
NM_021957.4:c.1423-15A>C MANE Select NP_068776.2:n.1423-15A>C
XM_006719063.3:c.1192-15A>C XP_006719126.1:n.1192-15A>C
XM_024448960.1:c.1423-15A>C XP_024304728.1:n.1423-15A>C