Canonical Allele Identifier: CA1814090592
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs1817905111

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111606T>C , CM000670.2:g.118111606T>C GRCh38
NC_000008.10:g.119123845T>C , CM000670.1:g.119123845T>C GRCh37
NC_000008.9:g.119193026T>C NCBI36
NG_007455.2:g.5214A>G , LRG_493:g.5214A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-560A>G MANE Select ENSP00000367446.3:n.-560A>G
ENST00000378204.6:c.-560A>G ENSP00000367446.2:n.-560A>G
NM_000127.2:c.-560A>G , LRG_493t1:c.-560A>G NP_000118.2:n.-560A>G
NM_000127.3:c.-560A>G MANE Select NP_000118.2:n.-560A>G