Canonical Allele Identifier: CA345014916

Gene: H3-3A

Linked Data

• MyVariant Identifiers: chr1:g.226252062A>G (hg19) ; chr1:g.226064361A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226064361A>G , CM000663.2:g.226064361A>G	GRCh38
NC_000001.10:g.226252062A>G , CM000663.1:g.226252062A>G	GRCh37
NC_000001.9:g.224318685A>G	NCBI36
NG_065173.1:g.6655A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366815.10:c.10A>G MANE Select	ENSP00000355780.3:p.Thr4Ala
ENST00000653960.1:n.119A>G
ENST00000655399.1:c.10A>G	ENSP00000499800.1:p.Thr4Ala
ENST00000656829.1:n.30-1374A>G
ENST00000661429.1:c.10A>G	ENSP00000499385.1:p.Thr4Ala
ENST00000666609.1:c.10A>G	ENSP00000499275.1:p.Thr4Ala
ENST00000667897.1:c.10A>G	ENSP00000499446.1:p.Thr4Ala
ENST00000366813.1:c.10A>G	ENSP00000355778.1:p.Thr4Ala
ENST00000366814.3:c.10A>G	ENSP00000355779.3:p.Thr4Ala
ENST00000366815.7:c.10A>G	ENSP00000355780.3:p.Thr4Ala
ENST00000366816.5:c.10A>G	ENSP00000355781.1:p.Thr4Ala
NM_002107.4:c.10A>G	NP_002098.1:p.Thr4Ala
NM_002107.5:c.10A>G	NP_002098.1:p.Thr4Ala
NM_002107.7:c.10A>G MANE Select	NP_002098.1:p.Thr4Ala
NM_001379043.1:c.10A>G	NP_001365972.1:p.Thr4Ala
NM_001379045.1:c.10A>G	NP_001365974.1:p.Thr4Ala
NM_001379046.1:c.10A>G	NP_001365975.1:p.Thr4Ala
NM_001379047.1:c.10A>G	NP_001365976.1:p.Thr4Ala