Canonical Allele Identifier: CA632121500

Gene: GCDH

Linked Data

• dbSNP Id: rs1440243697
• gnomAD v2: 19-13006984-C-T
• gnomAD v4: 19-12896170-C-T
• MyVariant Identifiers: chr19:g.13006984C>T (hg19) ; chr19:g.12896170C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896170C>T , CM000681.2:g.12896170C>T	GRCh38
NC_000019.9:g.13006984C>T , CM000681.1:g.13006984C>T	GRCh37
NC_000019.8:g.12867984C>T	NCBI36
NG_009292.1:g.10011C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.636-35C>T MANE Select	ENSP00000222214.4:n.636-35C>T
ENST00000222214.9:c.636-35C>T	ENSP00000222214.4:n.636-35C>T
ENST00000421816.6:n.614-35C>T
ENST00000585420.5:n.1000+49C>T
ENST00000590530.5:c.*76-35C>T	ENSP00000468452.1:n.*76-35C>T
ENST00000591043.1:n.672-35C>T
ENST00000591470.5:c.636-35C>T	ENSP00000466845.1:n.636-35C>T
NM_000159.3:c.636-35C>T	NP_000150.1:n.636-35C>T
NM_013976.3:c.636-35C>T	NP_039663.1:n.636-35C>T
NR_102316.1:n.799-35C>T
NR_102317.1:n.1051+49C>T
XM_006722721.2:c.636-35C>T	XP_006722784.1:n.636-35C>T
XM_011527899.1:c.636-35C>T	XP_011526201.1:n.636-35C>T
XM_011527900.1:c.636-35C>T	XP_011526202.1:n.636-35C>T
XM_011527899.2:c.636-35C>T	XP_011526201.1:n.636-35C>T
XM_011527900.2:c.636-35C>T	XP_011526202.1:n.636-35C>T
XM_017026580.1:c.636-35C>T	XP_016882069.1:n.636-35C>T
NM_000159.4:c.636-35C>T MANE Select	NP_000150.1:n.636-35C>T
NM_013976.4:c.636-35C>T	NP_039663.1:n.636-35C>T
NM_013976.5:c.636-35C>T	NP_039663.1:n.636-35C>T