Canonical Allele Identifier: CA184298142

Gene: EXT1

Linked Data

• dbSNP Id: rs879009226
• MyVariant Identifiers: chr8:g.118849438T>C (hg19) ; chr8:g.117837199T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117837199T>C , CM000670.2:g.117837199T>C	GRCh38
NC_000008.10:g.118849438T>C , CM000670.1:g.118849438T>C	GRCh37
NC_000008.9:g.118918619T>C	NCBI36
NG_007455.2:g.279621A>G , LRG_493:g.279621A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.432A>G
ENST00000378204.7:c.965A>G MANE Select	ENSP00000367446.3:p.Tyr322Cys
ENST00000436216.2:c.333A>G
ENST00000378204.6:c.965A>G	ENSP00000367446.2:p.Tyr322Cys
ENST00000436216.1:c.333A>G
ENST00000437196.1:c.74-1648A>G	ENSP00000407299.1:n.74-1648A>G
NM_000127.2:c.965A>G , LRG_493t1:c.965A>G	NP_000118.2:p.Tyr322Cys
NM_000127.3:c.965A>G MANE Select	NP_000118.2:p.Tyr322Cys