Canonical Allele Identifier: CA1118345065
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs1812198985
gnomAD v3: 8-117837078-C-T
gnomAD v4: 8-117837078-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837078C>T , CM000670.2:g.117837078C>T GRCh38
NC_000008.10:g.118849317C>T , CM000670.1:g.118849317C>T GRCh37
NC_000008.9:g.118918498C>T NCBI36
NG_007455.2:g.279742G>A , LRG_493:g.279742G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.523+30G>A
ENST00000378204.7:c.1056+30G>A MANE Select ENSP00000367446.3:n.1056+30G>A
ENST00000436216.2:c.424+30G>A
ENST00000378204.6:c.1056+30G>A ENSP00000367446.2:n.1056+30G>A
ENST00000436216.1:c.424+30G>A
ENST00000437196.1:c.74-1527G>A ENSP00000407299.1:n.74-1527G>A
NM_000127.2:c.1056+30G>A , LRG_493t1:c.1056+30G>A NP_000118.2:n.1056+30G>A
NM_000127.3:c.1056+30G>A MANE Select NP_000118.2:n.1056+30G>A
Search 100 bp 5'
Search 100 bp 3'