Canonical Allele Identifier: CA584341388

Gene: EXT1

Linked Data

• dbSNP Id: rs1289253063
• gnomAD v2: 8-118849325-G-A
• gnomAD v3: 8-117837086-G-A
• gnomAD v4: 8-117837086-G-A
• MyVariant Identifiers: chr8:g.118849325G>A (hg19) ; chr8:g.117837086G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117837086G>A , CM000670.2:g.117837086G>A	GRCh38
NC_000008.10:g.118849325G>A , CM000670.1:g.118849325G>A	GRCh37
NC_000008.9:g.118918506G>A	NCBI36
NG_007455.2:g.279734C>T , LRG_493:g.279734C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684189.1:n.523+22C>T
ENST00000378204.7:c.1056+22C>T MANE Select	ENSP00000367446.3:n.1056+22C>T
ENST00000436216.2:c.424+22C>T
ENST00000378204.6:c.1056+22C>T	ENSP00000367446.2:n.1056+22C>T
ENST00000436216.1:c.424+22C>T
ENST00000437196.1:c.74-1535C>T	ENSP00000407299.1:n.74-1535C>T
NM_000127.2:c.1056+22C>T , LRG_493t1:c.1056+22C>T	NP_000118.2:n.1056+22C>T
NM_000127.3:c.1056+22C>T MANE Select	NP_000118.2:n.1056+22C>T