Canonical Allele Identifier: CA2021167178
Gene: GYS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21546555C= , CM000674.2:g.21546555C= GRCh38
NC_000012.11:g.21699489C= , CM000674.1:g.21699489C= GRCh37
NC_000012.10:g.21590756C= NCBI36
NG_016167.1:g.63293G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261195.3:c.1423-85G= MANE Select ENSP00000261195.2:n.1423-85G=
ENST00000647960.1:c.*1425-85G= ENSP00000497202.1:n.*1425-85G=
ENST00000261195.2:c.1423-85G= ENSP00000261195.2:n.1423-85G=
NM_021957.3:c.1423-85G= NP_068776.2:n.1423-85G=
XM_005253352.1:c.1423-85G= XP_005253409.1:n.1423-85G=
XM_005253354.2:c.1204-85G= XP_005253411.1:n.1204-85G=
XM_006719062.2:c.1423-85G= XP_006719125.1:n.1423-85G=
XM_006719063.2:c.1192-85G= XP_006719126.1:n.1192-85G=
NM_021957.4:c.1423-85G= MANE Select NP_068776.2:n.1423-85G=
XM_006719063.3:c.1192-85G= XP_006719126.1:n.1192-85G=
XM_024448960.1:c.1423-85G= XP_024304728.1:n.1423-85G=
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