Canonical Allele Identifier: CA14719416

Gene: CDC37

Linked Data

• dbSNP Id: rs11879191
• gnomAD v2: 19-10512911-G-A
• gnomAD v3: 19-10402235-G-A
• gnomAD v4: 19-10402235-G-A
• MyVariant Identifiers: chr19:g.10512911G>A (hg19) ; chr19:g.10402235G>A (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10402235G>A , CM000681.2:g.10402235G>A	GRCh38
NC_000019.9:g.10512911G>A , CM000681.1:g.10512911G>A	GRCh37
NC_000019.8:g.10373911G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000222005.7:c.102+1143C>T MANE Select	ENSP00000222005.1:n.102+1143C>T
ENST00000222005.6:c.102+1143C>T	ENSP00000222005.1:n.102+1143C>T
ENST00000588869.1:c.102+1143C>T	ENSP00000464971.1:n.102+1143C>T
ENST00000589629.5:c.102+1143C>T	ENSP00000467747.1:n.102+1143C>T
ENST00000591248.5:n.153+1143C>T
ENST00000593124.1:c.102+1143C>T	ENSP00000465724.1:n.102+1143C>T
NM_007065.3:c.102+1143C>T	NP_008996.1:n.102+1143C>T
XM_011527652.1:c.102+1143C>T	XP_011525954.1:n.102+1143C>T
XM_011527652.3:c.102+1143C>T	XP_011525954.1:n.102+1143C>T
NM_007065.4:c.102+1143C>T MANE Select	NP_008996.1:n.102+1143C>T