Canonical Allele Identifier: CA462465224
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs1563873618
MyVariant Identifiers: chr8:g.118819587G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117807348G>A , CM000670.2:g.117807348G>A GRCh38
NC_000008.10:g.118819587G>A , CM000670.1:g.118819587G>A GRCh37
NC_000008.9:g.118888768G>A NCBI36
NG_007455.2:g.309472C>T , LRG_493:g.309472C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.1219C>T
ENST00000378204.7:c.1752C>T MANE Select ENSP00000367446.3:p.Ser584=
ENST00000378204.6:c.1752C>T ENSP00000367446.2:p.Ser584=
ENST00000437196.1:c.*643C>T ENSP00000407299.1:n.*643C>T
NM_000127.2:c.1752C>T , LRG_493t1:c.1752C>T NP_000118.2:p.Ser584=
NM_000127.3:c.1752C>T MANE Select NP_000118.2:p.Ser584=