Canonical Allele Identifier: CA4854261
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs374554042
ExAC: 8:118849306 G / T
gnomAD v2: 8-118849306-G-T
gnomAD v3: 8-117837067-G-T
gnomAD v4: 8-117837067-G-T
MyVariant Identifiers: chr8:g.118849306G>T (hg19) chr8:g.117837067G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837067G>T , CM000670.2:g.117837067G>T GRCh38
NC_000008.10:g.118849306G>T , CM000670.1:g.118849306G>T GRCh37
NC_000008.9:g.118918487G>T NCBI36
NG_007455.2:g.279753C>A , LRG_493:g.279753C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.523+41C>A
ENST00000378204.7:c.1056+41C>A MANE Select ENSP00000367446.3:n.1056+41C>A
ENST00000436216.2:c.424+41C>A
ENST00000378204.6:c.1056+41C>A ENSP00000367446.2:n.1056+41C>A
ENST00000436216.1:c.424+41C>A
ENST00000437196.1:c.74-1516C>A ENSP00000407299.1:n.74-1516C>A
NM_000127.2:c.1056+41C>A , LRG_493t1:c.1056+41C>A NP_000118.2:n.1056+41C>A
NM_000127.3:c.1056+41C>A MANE Select NP_000118.2:n.1056+41C>A
Search 100 bp 5'
Search 100 bp 3'