Canonical Allele Identifier: CA371914692
Gene: EXT1 HGNC NCBI

Linked Data

gnomAD v4: 8-118110101-T-C
MyVariant Identifiers: chr8:g.119122340T>C (hg19) chr8:g.118110101T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118110101T>C , CM000670.2:g.118110101T>C GRCh38
NC_000008.10:g.119122340T>C , CM000670.1:g.119122340T>C GRCh37
NC_000008.9:g.119191521T>C NCBI36
NG_007455.2:g.6719A>G , LRG_493:g.6719A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.946A>G MANE Select ENSP00000367446.3:p.Asn316Asp
ENST00000436216.2:c.314A>G
ENST00000378204.6:c.946A>G ENSP00000367446.2:p.Asn316Asp
ENST00000436216.1:c.314A>G
ENST00000437196.1:c.73+873A>G ENSP00000407299.1:n.73+873A>G
NM_000127.2:c.946A>G , LRG_493t1:c.946A>G NP_000118.2:p.Asn316Asp
NM_000127.3:c.946A>G MANE Select NP_000118.2:p.Asn316Asp
Search 100 bp 5'
Search 100 bp 3'