Canonical Allele Identifier: CA1814090562
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs1817904438

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111563T>A , CM000670.2:g.118111563T>A GRCh38
NC_000008.10:g.119123802T>A , CM000670.1:g.119123802T>A GRCh37
NC_000008.9:g.119192983T>A NCBI36
NG_007455.2:g.5257A>T , LRG_493:g.5257A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-517A>T MANE Select ENSP00000367446.3:n.-517A>T
ENST00000378204.6:c.-517A>T ENSP00000367446.2:n.-517A>T
NM_000127.2:c.-517A>T , LRG_493t1:c.-517A>T NP_000118.2:n.-517A>T
NM_000127.3:c.-517A>T MANE Select NP_000118.2:n.-517A>T