Canonical Allele Identifier: CA478869547
Gene: GYS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21715954A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21563020A>C , CM000674.2:g.21563020A>C GRCh38
NC_000012.11:g.21715954A>C , CM000674.1:g.21715954A>C GRCh37
NC_000012.10:g.21607221A>C NCBI36
NG_016167.1:g.46828T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261195.3:c.960T>G MANE Select ENSP00000261195.2:p.Leu320=
ENST00000647960.1:c.*962T>G ENSP00000497202.1:n.*962T>G
ENST00000648372.1:n.887T>G
ENST00000261195.2:c.960T>G ENSP00000261195.2:p.Leu320=
NM_021957.3:c.960T>G NP_068776.2:p.Leu320=
XM_005253352.1:c.960T>G XP_005253409.1:p.Leu320=
XM_005253354.2:c.741T>G XP_005253411.1:p.Leu247=
XM_006719062.2:c.960T>G XP_006719125.1:p.Leu320=
XM_006719063.2:c.729T>G XP_006719126.1:p.Leu243=
NM_021957.4:c.960T>G MANE Select NP_068776.2:p.Leu320=
XM_006719063.3:c.729T>G XP_006719126.1:p.Leu243=
XM_017019245.2:c.960T>G XP_016874734.1:p.Leu320=
XM_024448960.1:c.960T>G XP_024304728.1:p.Leu320=