Canonical Allele Identifier: CA603667866
Gene: GYS2 HGNC NCBI

Linked Data

dbSNP Id: rs1410584838
gnomAD v2: 12-21699403-AC-A
gnomAD v4: 12-21546469-AC-A
MyVariant Identifiers: chr12:g.21699404del (hg19) chr12:g.21546470del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21546471del , CM000674.2:g.21546471del GRCh38
NC_000012.11:g.21699405del , CM000674.1:g.21699405del GRCh37
NC_000012.10:g.21590672del NCBI36
NG_016167.1:g.63378del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261195.3:c.1423del
ENST00000647960.1:c.*1425del
ENST00000261195.2:c.1423del
NM_021957.3:c.1423del
XM_005253352.1:c.1423del
XM_005253354.2:c.1204del
XM_006719062.2:c.1423del
XM_006719063.2:c.1192del
NM_021957.4:c.1423del
XM_006719063.3:c.1192del
XM_024448960.1:c.1423del
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