Canonical Allele Identifier: CA16602872

Gene: H3C11

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.27872234T>C , CM000668.2:g.27872234T>C	GRCh38
NC_000006.11:g.27840012T>C , CM000668.1:g.27840012T>C	GRCh37
NC_000006.10:g.27947991T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616365.2:c.82A>G MANE Select	ENSP00000483283.2:p.Lys28Glu
ENST00000616365.1:c.82A>G	ENSP00000483283.1:p.Lys28Glu
NM_003533.2:c.82A>G	NP_003524.1:p.Lys28Glu
NM_003533.3:c.82A>G MANE Select	NP_003524.1:p.Lys28Glu