Canonical Allele Identifier: CA352906460

Gene: HYAL2

Linked Data

• dbSNP Id: rs1553716136
• gnomAD v4: 3-50319567-A-G
• MyVariant Identifiers: chr3:g.50356998A>G (hg19) ; chr3:g.50319567A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50319567A>G , CM000665.2:g.50319567A>G	GRCh38
NC_000003.11:g.50356998A>G , CM000665.1:g.50356998A>G	GRCh37
NC_000003.10:g.50332002A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357750.9:c.921+2T>C MANE Select	ENSP00000350387.4:n.921+2T>C
ENST00000357750.8:c.921+2T>C	ENSP00000350387.4:n.921+2T>C
ENST00000395139.7:c.921+2T>C	ENSP00000378571.3:n.921+2T>C
ENST00000442581.1:c.921+2T>C	ENSP00000406657.1:n.921+2T>C
ENST00000447092.5:c.921+2T>C	ENSP00000401853.1:n.921+2T>C
ENST00000481597.5:n.1056+2T>C
NM_003773.4:c.921+2T>C	NP_003764.3:n.921+2T>C
NM_033158.4:c.921+2T>C	NP_149348.2:n.921+2T>C
XM_005265524.1:c.921+2T>C	XP_005265581.1:n.921+2T>C
XM_005265525.1:c.921+2T>C	XP_005265582.1:n.921+2T>C
XM_005265524.2:c.921+2T>C	XP_005265581.1:n.921+2T>C
XM_005265525.2:c.921+2T>C	XP_005265582.1:n.921+2T>C
NM_003773.5:c.921+2T>C MANE Select	NP_003764.3:n.921+2T>C
NM_033158.5:c.921+2T>C	NP_149348.2:n.921+2T>C