Canonical Allele Identifier: CA352907068

Gene: HYAL2

Linked Data

• gnomAD v4: 3-50319654-G-C
• MyVariant Identifiers: chr3:g.50357085G>C (hg19) ; chr3:g.50319654G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50319654G>C , CM000665.2:g.50319654G>C	GRCh38
NC_000003.11:g.50357085G>C , CM000665.1:g.50357085G>C	GRCh37
NC_000003.10:g.50332089G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357750.9:c.836C>G MANE Select	ENSP00000350387.4:p.Ala279Gly
ENST00000357750.8:c.836C>G	ENSP00000350387.4:p.Ala279Gly
ENST00000395139.7:c.836C>G	ENSP00000378571.3:p.Ala279Gly
ENST00000442581.1:c.836C>G	ENSP00000406657.1:p.Ala279Gly
ENST00000447092.5:c.836C>G	ENSP00000401853.1:p.Ala279Gly
ENST00000481597.5:n.971C>G
NM_003773.4:c.836C>G	NP_003764.3:p.Ala279Gly
NM_033158.4:c.836C>G	NP_149348.2:p.Ala279Gly
XM_005265524.1:c.836C>G	XP_005265581.1:p.Ala279Gly
XM_005265525.1:c.836C>G	XP_005265582.1:p.Ala279Gly
XM_005265524.2:c.836C>G	XP_005265581.1:p.Ala279Gly
XM_005265525.2:c.836C>G	XP_005265582.1:p.Ala279Gly
NM_003773.5:c.836C>G MANE Select	NP_003764.3:p.Ala279Gly
NM_033158.5:c.836C>G	NP_149348.2:p.Ala279Gly