Canonical Allele Identifier: CA345016065

Gene: H3-3A

Linked Data

• ClinVar Variation Id: 985690
• ClinVar RCV Id: RCV001266726
• dbSNP Id: rs1576199734
• MyVariant Identifiers: chr1:g.226252159T>C (hg19) ; chr1:g.226064458T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226064458T>C , CM000663.2:g.226064458T>C	GRCh38
NC_000001.10:g.226252159T>C , CM000663.1:g.226252159T>C	GRCh37
NC_000001.9:g.224318782T>C	NCBI36
NG_065173.1:g.6752T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366815.10:c.107T>C MANE Select	ENSP00000355780.3:p.Val36Ala
ENST00000653960.1:n.216T>C
ENST00000655399.1:c.107T>C	ENSP00000499800.1:p.Val36Ala
ENST00000656829.1:n.30-1277T>C
ENST00000661429.1:c.107T>C	ENSP00000499385.1:p.Val36Ala
ENST00000666609.1:c.107T>C	ENSP00000499275.1:p.Val36Ala
ENST00000667897.1:c.107T>C	ENSP00000499446.1:p.Val36Ala
ENST00000366813.1:c.107T>C	ENSP00000355778.1:p.Val36Ala
ENST00000366814.3:c.107T>C	ENSP00000355779.3:p.Val36Ala
ENST00000366815.7:c.107T>C	ENSP00000355780.3:p.Val36Ala
ENST00000366816.5:c.107T>C	ENSP00000355781.1:p.Val36Ala
NM_002107.4:c.107T>C	NP_002098.1:p.Val36Ala
NM_002107.5:c.107T>C	NP_002098.1:p.Val36Ala
NM_002107.7:c.107T>C MANE Select	NP_002098.1:p.Val36Ala
NM_001379043.1:c.107T>C	NP_001365972.1:p.Val36Ala
NM_001379045.1:c.107T>C	NP_001365974.1:p.Val36Ala
NM_001379046.1:c.107T>C	NP_001365975.1:p.Val36Ala
NM_001379047.1:c.107T>C	NP_001365976.1:p.Val36Ala