Canonical Allele Identifier: CA2650752342

Gene: H3-3A

Linked Data

• gnomAD v4: 1-226064351-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226064351C>A , CM000663.2:g.226064351C>A	GRCh38
NC_000001.10:g.226252052C>A , CM000663.1:g.226252052C>A	GRCh37
NC_000001.9:g.224318675C>A	NCBI36
NG_065173.1:g.6645C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366815.10:c.-1C>A MANE Select	ENSP00000355780.3:n.-1C>A
ENST00000653960.1:n.109C>A
ENST00000655399.1:c.-1C>A	ENSP00000499800.1:n.-1C>A
ENST00000656829.1:n.30-1384C>A
ENST00000661429.1:c.-1C>A	ENSP00000499385.1:n.-1C>A
ENST00000666609.1:c.-1C>A	ENSP00000499275.1:n.-1C>A
ENST00000667897.1:c.-1C>A	ENSP00000499446.1:n.-1C>A
ENST00000366813.1:c.-1C>A	ENSP00000355778.1:n.-1C>A
ENST00000366814.3:c.-1C>A	ENSP00000355779.3:n.-1C>A
ENST00000366815.7:c.-1C>A	ENSP00000355780.3:n.-1C>A
ENST00000366816.5:c.-1C>A	ENSP00000355781.1:n.-1C>A
NM_002107.4:c.-1C>A	NP_002098.1:n.-1C>A
NM_002107.5:c.-1C>A	NP_002098.1:n.-1C>A
NM_002107.7:c.-1C>A MANE Select	NP_002098.1:n.-1C>A
NM_001379043.1:c.-1C>A	NP_001365972.1:n.-1C>A
NM_001379045.1:c.-1C>A	NP_001365974.1:n.-1C>A
NM_001379046.1:c.-1C>A	NP_001365975.1:n.-1C>A
NM_001379047.1:c.-1C>A	NP_001365976.1:n.-1C>A