Canonical Allele Identifier: CA1814090558
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs1817904328

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111559A>C , CM000670.2:g.118111559A>C GRCh38
NC_000008.10:g.119123798A>C , CM000670.1:g.119123798A>C GRCh37
NC_000008.9:g.119192979A>C NCBI36
NG_007455.2:g.5261T>G , LRG_493:g.5261T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-513T>G MANE Select ENSP00000367446.3:n.-513T>G
ENST00000378204.6:c.-513T>G ENSP00000367446.2:n.-513T>G
NM_000127.2:c.-513T>G , LRG_493t1:c.-513T>G NP_000118.2:n.-513T>G
NM_000127.3:c.-513T>G MANE Select NP_000118.2:n.-513T>G