Canonical Allele Identifier: CA5954993
Gene: EXT2 HGNC NCBI

Linked Data

dbSNP Id: rs758788938

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44124770C>G , CM000673.2:g.44124770C>G GRCh38
NC_000011.9:g.44146320C>G , CM000673.1:g.44146320C>G GRCh37
NC_000011.8:g.44102896C>G NCBI36
NG_007560.1:g.34222C>G , LRG_494:g.34222C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343631.4:c.744-19C>G ENSP00000342656.3:n.744-19C>G
ENST00000395673.8:c.744-19C>G ENSP00000379032.4:n.744-19C>G
ENST00000531161.6:n.903-19C>G
ENST00000682359.1:c.744-19C>G ENSP00000508226.1:n.744-19C>G
ENST00000682711.1:c.-544+28918C>G ENSP00000506803.1:n.-544+28918C>G
ENST00000682815.1:c.744-19C>G ENSP00000507234.1:n.744-19C>G
ENST00000682947.1:n.918-19C>G
ENST00000682993.1:c.744-19C>G ENSP00000507580.1:n.744-19C>G
ENST00000683000.1:c.744-19C>G ENSP00000508361.1:n.744-19C>G
ENST00000683299.1:n.1161-19C>G
ENST00000683870.1:c.744-19C>G ENSP00000507922.1:n.744-19C>G
ENST00000683881.1:n.3305-19C>G
ENST00000684039.1:c.744-19C>G ENSP00000507677.1:n.744-19C>G
ENST00000684124.1:c.744-19C>G ENSP00000508332.1:n.744-19C>G
ENST00000684533.1:c.744-5275C>G ENSP00000507915.1:n.744-5275C>G
ENST00000533608.7:c.744-19C>G MANE Select ENSP00000431173.2:n.744-19C>G
ENST00000343631.3:c.744-19C>G ENSP00000342656.3:n.744-19C>G
ENST00000358681.8:c.744-19C>G ENSP00000351509.4:n.744-19C>G
ENST00000395673.7:c.843-19C>G ENSP00000379032.3:n.843-19C>G
ENST00000533608.5:c.744-19C>G ENSP00000431173.1:n.744-19C>G
NM_000401.3:c.843-19C>G , LRG_494t1:c.843-19C>G NP_000392.3:n.843-19C>G
NM_001178083.1:c.744-19C>G NP_001171554.1:n.744-19C>G
NM_207122.1:c.744-19C>G , LRG_494t2:c.744-19C>G NP_997005.1:n.744-19C>G
XM_011519950.1:c.882-19C>G XP_011518252.1:n.882-19C>G
XM_011519951.1:c.783-19C>G XP_011518253.1:n.783-19C>G
XM_024448383.1:c.882-19C>G XP_024304151.1:n.882-19C>G
NM_001178083.2:c.744-19C>G NP_001171554.1:n.744-19C>G
NM_207122.2:c.744-19C>G MANE Select NP_997005.1:n.744-19C>G
NM_001178083.3:c.744-19C>G NP_001171554.1:n.744-19C>G
NM_001389628.1:c.744-19C>G NP_001376557.1:n.744-19C>G
NM_001389630.1:c.744-19C>G NP_001376559.1:n.744-19C>G