Canonical Allele Identifier: CA10588450
Gene: EXT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 265127
ClinVar RCV Id: RCV000256094 RCV001224730
dbSNP Id: rs886039353
COSMIC: COSM1205858
MyVariant Identifiers: chr8:g.119122323C>A (hg19) chr8:g.118110084C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118110084C>A , CM000670.2:g.118110084C>A GRCh38
NC_000008.10:g.119122323C>A , CM000670.1:g.119122323C>A GRCh37
NC_000008.9:g.119191504C>A NCBI36
NG_007455.2:g.6736G>T , LRG_493:g.6736G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378204.7:c.962+1G>T MANE Select ENSP00000367446.3:n.962+1G>T
ENST00000436216.2:c.330+1G>T
ENST00000378204.6:c.962+1G>T ENSP00000367446.2:n.962+1G>T
ENST00000436216.1:c.330+1G>T
ENST00000437196.1:c.73+890G>T ENSP00000407299.1:n.73+890G>T
NM_000127.2:c.962+1G>T , LRG_493t1:c.962+1G>T NP_000118.2:n.962+1G>T
NM_000127.3:c.962+1G>T MANE Select NP_000118.2:n.962+1G>T
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