Canonical Allele Identifier: CA936784

Gene: HS2ST1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.87084175A>G , CM000663.2:g.87084175A>G	GRCh38
NC_000001.10:g.87549858A>G , CM000663.1:g.87549858A>G	GRCh37
NC_000001.9:g.87322446A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012262.4:c.364-19A>G MANE Select	NP_036394.1:n.364-19A>G
ENST00000370550.10:c.364-19A>G MANE Select	ENSP00000359581.4:n.364-19A>G
NM_001134492.1:c.364-19A>G	NP_001127964.1:n.364-19A>G
NM_001134492.2:c.364-19A>G	NP_001127964.1:n.364-19A>G
NM_012262.3:c.364-19A>G	NP_036394.1:n.364-19A>G
ENST00000370548.3:c.286-19A>G	ENSP00000359579.1:n.286-19A>G
ENST00000370550.9:c.364-19A>G	ENSP00000359581.4:n.364-19A>G
ENST00000370551.8:c.364-19A>G	ENSP00000359582.3:n.364-19A>G
ENST00000591456.1:c.190-19A>G	ENSP00000467253.1:n.190-19A>G
ENST00000687893.1:c.364-19A>G	ENSP00000508894.1:n.364-19A>G
ENST00000689904.1:c.364-19A>G	ENSP00000509983.1:n.364-19A>G
ENST00000690674.1:c.190-19A>G	ENSP00000509377.1:n.190-19A>G
ENST00000693745.1:c.*340-19A>G	ENSP00000509333.1:n.*340-19A>G