Canonical Allele Identifier: CA367654933

Gene: GUSB

Linked Data

• dbSNP Id: rs1420444944
• gnomAD v3: 7-65982038-G-A
• gnomAD v4: 7-65982038-G-A
• MyVariant Identifiers: chr7:g.65447025G>A (hg19) ; chr7:g.65982038G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65982038G>A , CM000669.2:g.65982038G>A	GRCh38
NC_000007.13:g.65447025G>A , CM000669.1:g.65447025G>A	GRCh37
NC_000007.12:g.65084460G>A	NCBI36
NG_016197.1:g.5277C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.146C>T MANE Select	ENSP00000302728.4:p.Ala49Val
ENST00000304895.8:c.146C>T	ENSP00000302728.4:p.Ala49Val
ENST00000421103.5:c.146C>T	ENSP00000391390.1:p.Ala49Val
ENST00000430730.5:c.146C>T	ENSP00000411859.1:p.Ala49Val
ENST00000446111.1:c.146C>T	ENSP00000416793.1:p.Ala49Val
ENST00000447929.5:c.146C>T	ENSP00000411262.1:p.Ala49Val
ENST00000475316.5:n.51C>T
NM_000181.3:c.146C>T	NP_000172.2:p.Ala49Val
NM_001284290.1:c.146C>T	NP_001271219.1:p.Ala49Val
NM_001293104.1:c.-240C>T	NP_001280033.1:n.-240C>T
NM_001293105.1:c.-184C>T	NP_001280034.1:n.-184C>T
NR_120531.1:n.277C>T
XM_005250297.3:c.146C>T	XP_005250354.1:p.Ala49Val
XM_011516113.1:c.-184C>T	XP_011514415.1:n.-184C>T
XR_927461.1:n.272C>T
XM_005250297.4:c.146C>T	XP_005250354.1:p.Ala49Val
XM_011516114.2:c.-540C>T	XP_011514416.1:n.-540C>T
XM_017012091.1:c.-184C>T	XP_016867580.1:n.-184C>T
XM_017012092.1:c.-240C>T	XP_016867581.1:n.-240C>T
XM_017012093.2:c.-540C>T	XP_016867582.1:n.-540C>T
XR_001744658.2:n.191C>T
XR_001744659.2:n.191C>T
XR_001744660.2:n.191C>T
XR_001744661.2:n.191C>T
XR_927461.3:n.191C>T
NM_000181.4:c.146C>T MANE Select	NP_000172.2:p.Ala49Val
NM_001284290.2:c.146C>T	NP_001271219.1:p.Ala49Val
NM_001293104.2:c.-240C>T	NP_001280033.1:n.-240C>T
NM_001293105.2:c.-184C>T	NP_001280034.1:n.-184C>T
NR_120531.2:n.176C>T