Canonical Allele Identifier: CA846256000
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs1357772428
MyVariant Identifiers: chr8:g.119123671T>C (hg19) chr8:g.118111432T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111432T>C , CM000670.2:g.118111432T>C GRCh38
NC_000008.10:g.119123671T>C , CM000670.1:g.119123671T>C GRCh37
NC_000008.9:g.119192852T>C NCBI36
NG_007455.2:g.5388A>G , LRG_493:g.5388A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378204.7:c.-386A>G MANE Select ENSP00000367446.3:n.-386A>G
ENST00000378204.6:c.-386A>G ENSP00000367446.2:n.-386A>G
NM_000127.2:c.-386A>G , LRG_493t1:c.-386A>G NP_000118.2:n.-386A>G
NM_000127.3:c.-386A>G MANE Select NP_000118.2:n.-386A>G
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