Canonical Allele Identifier: CA9234449

Gene: GCDH

Linked Data

• ClinVar Variation Id: 555620
• ClinVar RCV Id: RCV000671476
• dbSNP Id: rs138216703
• ExAC: 19:13006981 G / A
• gnomAD v2: 19-13006981-G-A
• gnomAD v3: 19-12896167-G-A
• gnomAD v4: 19-12896167-G-A
• MyVariant Identifiers: chr19:g.13006981G>A (hg19) ; chr19:g.12896167G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896167G>A , CM000681.2:g.12896167G>A	GRCh38
NC_000019.9:g.13006981G>A , CM000681.1:g.13006981G>A	GRCh37
NC_000019.8:g.12867981G>A	NCBI36
NG_009292.1:g.10008G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.636-38G>A MANE Select	ENSP00000222214.4:n.636-38G>A
ENST00000222214.9:c.636-38G>A	ENSP00000222214.4:n.636-38G>A
ENST00000421816.6:n.614-38G>A
ENST00000585420.5:n.1000+46G>A
ENST00000590530.5:c.*76-38G>A	ENSP00000468452.1:n.*76-38G>A
ENST00000591043.1:n.672-38G>A
ENST00000591470.5:c.636-38G>A	ENSP00000466845.1:n.636-38G>A
NM_000159.3:c.636-38G>A	NP_000150.1:n.636-38G>A
NM_013976.3:c.636-38G>A	NP_039663.1:n.636-38G>A
NR_102316.1:n.799-38G>A
NR_102317.1:n.1051+46G>A
XM_006722721.2:c.636-38G>A	XP_006722784.1:n.636-38G>A
XM_011527899.1:c.636-38G>A	XP_011526201.1:n.636-38G>A
XM_011527900.1:c.636-38G>A	XP_011526202.1:n.636-38G>A
XM_011527899.2:c.636-38G>A	XP_011526201.1:n.636-38G>A
XM_011527900.2:c.636-38G>A	XP_011526202.1:n.636-38G>A
XM_017026580.1:c.636-38G>A	XP_016882069.1:n.636-38G>A
NM_000159.4:c.636-38G>A MANE Select	NP_000150.1:n.636-38G>A
NM_013976.4:c.636-38G>A	NP_039663.1:n.636-38G>A
NM_013976.5:c.636-38G>A	NP_039663.1:n.636-38G>A