Canonical Allele Identifier: CA6480024
Gene: GYS2 HGNC NCBI

Linked Data

dbSNP Id: rs759499770

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21562976G>A , CM000674.2:g.21562976G>A GRCh38
NC_000012.11:g.21715910G>A , CM000674.1:g.21715910G>A GRCh37
NC_000012.10:g.21607177G>A NCBI36
NG_016167.1:g.46872C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261195.3:c.1004C>T MANE Select ENSP00000261195.2:p.Ser335Leu
ENST00000647960.1:c.*1006C>T ENSP00000497202.1:n.*1006C>T
ENST00000648372.1:n.931C>T
ENST00000261195.2:c.1004C>T ENSP00000261195.2:p.Ser335Leu
NM_021957.3:c.1004C>T NP_068776.2:p.Ser335Leu
XM_005253352.1:c.1004C>T XP_005253409.1:p.Ser335Leu
XM_005253354.2:c.785C>T XP_005253411.1:p.Ser262Leu
XM_006719062.2:c.1004C>T XP_006719125.1:p.Ser335Leu
XM_006719063.2:c.773C>T XP_006719126.1:p.Ser258Leu
NM_021957.4:c.1004C>T MANE Select NP_068776.2:p.Ser335Leu
XM_006719063.3:c.773C>T XP_006719126.1:p.Ser258Leu
XM_017019245.2:c.1004C>T XP_016874734.1:p.Ser335Leu
XM_024448960.1:c.1004C>T XP_024304728.1:p.Ser335Leu