Canonical Allele Identifier: CA380179966

Gene: EXT2

Linked Data

• dbSNP Id: rs2134966881
• gnomAD v4: 11-44107974-C-T
• MyVariant Identifiers: chr11:g.44129524C>T (hg19) ; chr11:g.44107974C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44107974C>T , CM000673.2:g.44107974C>T	GRCh38
NC_000011.9:g.44129524C>T , CM000673.1:g.44129524C>T	GRCh37
NC_000011.8:g.44086100C>T	NCBI36
NG_007560.1:g.17426C>T , LRG_494:g.17426C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.262C>T	ENSP00000342656.3:p.His88Tyr
ENST00000395673.8:c.262C>T	ENSP00000379032.4:p.His88Tyr
ENST00000531161.6:n.421C>T
ENST00000682359.1:c.262C>T	ENSP00000508226.1:p.His88Tyr
ENST00000682711.1:c.-544+12122C>T	ENSP00000506803.1:n.-544+12122C>T
ENST00000682815.1:c.262C>T	ENSP00000507234.1:p.His88Tyr
ENST00000682947.1:n.436C>T
ENST00000682993.1:c.262C>T	ENSP00000507580.1:p.His88Tyr
ENST00000683000.1:c.262C>T	ENSP00000508361.1:p.His88Tyr
ENST00000683299.1:n.679C>T
ENST00000683870.1:c.262C>T	ENSP00000507922.1:p.His88Tyr
ENST00000683881.1:n.2823C>T
ENST00000684039.1:c.262C>T	ENSP00000507677.1:p.His88Tyr
ENST00000684124.1:c.262C>T	ENSP00000508332.1:p.His88Tyr
ENST00000684533.1:c.262C>T	ENSP00000507915.1:p.His88Tyr
ENST00000533608.7:c.262C>T MANE Select	ENSP00000431173.2:p.His88Tyr
ENST00000343631.3:c.262C>T	ENSP00000342656.3:p.His88Tyr
ENST00000358681.8:c.262C>T	ENSP00000351509.4:p.His88Tyr
ENST00000395673.7:c.361C>T	ENSP00000379032.3:p.His121Tyr
ENST00000527014.1:c.262C>T	ENSP00000434716.1:p.His88Tyr
ENST00000533608.5:c.262C>T	ENSP00000431173.1:p.His88Tyr
NM_000401.3:c.361C>T , LRG_494t1:c.361C>T	NP_000392.3:p.His121Tyr
NM_001178083.1:c.262C>T	NP_001171554.1:p.His88Tyr
NM_207122.1:c.262C>T , LRG_494t2:c.262C>T	NP_997005.1:p.His88Tyr
XM_011519950.1:c.400C>T	XP_011518252.1:p.His134Tyr
XM_011519951.1:c.301C>T	XP_011518253.1:p.His101Tyr
XM_024448383.1:c.400C>T	XP_024304151.1:p.His134Tyr
NM_001178083.2:c.262C>T	NP_001171554.1:p.His88Tyr
NM_207122.2:c.262C>T MANE Select	NP_997005.1:p.His88Tyr
NM_001178083.3:c.262C>T	NP_001171554.1:p.His88Tyr
NM_001389628.1:c.262C>T	NP_001376557.1:p.His88Tyr
NM_001389630.1:c.262C>T	NP_001376559.1:p.His88Tyr