Canonical Allele Identifier: CA462645054
Gene: EXT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.119122398G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118110159G>C , CM000670.2:g.118110159G>C GRCh38
NC_000008.10:g.119122398G>C , CM000670.1:g.119122398G>C GRCh37
NC_000008.9:g.119191579G>C NCBI36
NG_007455.2:g.6661C>G , LRG_493:g.6661C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378204.7:c.888C>G MANE Select ENSP00000367446.3:p.Thr296=
ENST00000436216.2:c.256C>G
ENST00000378204.6:c.888C>G ENSP00000367446.2:p.Thr296=
ENST00000436216.1:c.256C>G
ENST00000437196.1:c.73+815C>G ENSP00000407299.1:n.73+815C>G
NM_000127.2:c.888C>G , LRG_493t1:c.888C>G NP_000118.2:p.Thr296=
NM_000127.3:c.888C>G MANE Select NP_000118.2:p.Thr296=
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