Canonical Allele Identifier: CA1118366822
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs1817904608

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111575G>A , CM000670.2:g.118111575G>A GRCh38
NC_000008.10:g.119123814G>A , CM000670.1:g.119123814G>A GRCh37
NC_000008.9:g.119192995G>A NCBI36
NG_007455.2:g.5245C>T , LRG_493:g.5245C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-529C>T MANE Select ENSP00000367446.3:n.-529C>T
ENST00000378204.6:c.-529C>T ENSP00000367446.2:n.-529C>T
NM_000127.2:c.-529C>T , LRG_493t1:c.-529C>T NP_000118.2:n.-529C>T
NM_000127.3:c.-529C>T MANE Select NP_000118.2:n.-529C>T