Canonical Allele Identifier: CA2688347262
Gene: EXT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111384A>C , CM000670.2:g.118111384A>C GRCh38
NC_000008.10:g.119123623A>C , CM000670.1:g.119123623A>C GRCh37
NC_000008.9:g.119192804A>C NCBI36
NG_007455.2:g.5436T>G , LRG_493:g.5436T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378204.7:c.-338T>G MANE Select ENSP00000367446.3:n.-338T>G
ENST00000378204.6:c.-338T>G ENSP00000367446.2:n.-338T>G
NM_000127.2:c.-338T>G , LRG_493t1:c.-338T>G NP_000118.2:n.-338T>G
NM_000127.3:c.-338T>G MANE Select NP_000118.2:n.-338T>G