Canonical Allele Identifier: CA345014891

Gene: H3-3A

Linked Data

• MyVariant Identifiers: chr1:g.226252056G>T (hg19) ; chr1:g.226064355G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226064355G>T , CM000663.2:g.226064355G>T	GRCh38
NC_000001.10:g.226252056G>T , CM000663.1:g.226252056G>T	GRCh37
NC_000001.9:g.224318679G>T	NCBI36
NG_065173.1:g.6649G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366815.10:c.4G>T MANE Select	ENSP00000355780.3:p.Ala2Ser
ENST00000653960.1:n.113G>T
ENST00000655399.1:c.4G>T	ENSP00000499800.1:p.Ala2Ser
ENST00000656829.1:n.30-1380G>T
ENST00000661429.1:c.4G>T	ENSP00000499385.1:p.Ala2Ser
ENST00000666609.1:c.4G>T	ENSP00000499275.1:p.Ala2Ser
ENST00000667897.1:c.4G>T	ENSP00000499446.1:p.Ala2Ser
ENST00000366813.1:c.4G>T	ENSP00000355778.1:p.Ala2Ser
ENST00000366814.3:c.4G>T	ENSP00000355779.3:p.Ala2Ser
ENST00000366815.7:c.4G>T	ENSP00000355780.3:p.Ala2Ser
ENST00000366816.5:c.4G>T	ENSP00000355781.1:p.Ala2Ser
NM_002107.4:c.4G>T	NP_002098.1:p.Ala2Ser
NM_002107.5:c.4G>T	NP_002098.1:p.Ala2Ser
NM_002107.7:c.4G>T MANE Select	NP_002098.1:p.Ala2Ser
NM_001379043.1:c.4G>T	NP_001365972.1:p.Ala2Ser
NM_001379045.1:c.4G>T	NP_001365974.1:p.Ala2Ser
NM_001379046.1:c.4G>T	NP_001365975.1:p.Ala2Ser
NM_001379047.1:c.4G>T	NP_001365976.1:p.Ala2Ser