Canonical Allele Identifier: CA1814090471
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs1586280717

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111466C>T , CM000670.2:g.118111466C>T GRCh38
NC_000008.10:g.119123705C>T , CM000670.1:g.119123705C>T GRCh37
NC_000008.9:g.119192886C>T NCBI36
NG_007455.2:g.5354G>A , LRG_493:g.5354G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-420G>A MANE Select ENSP00000367446.3:n.-420G>A
ENST00000378204.6:c.-420G>A ENSP00000367446.2:n.-420G>A
NM_000127.2:c.-420G>A , LRG_493t1:c.-420G>A NP_000118.2:n.-420G>A
NM_000127.3:c.-420G>A MANE Select NP_000118.2:n.-420G>A