Canonical Allele Identifier: CA2323620985
Gene: GCDH HGNC NCBI

Linked Data

dbSNP Id: rs1970558082

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12891597C>G , CM000681.2:g.12891597C>G GRCh38
NC_000019.9:g.13002411C>G , CM000681.1:g.13002411C>G GRCh37
NC_000019.8:g.12863411C>G NCBI36
NG_009292.1:g.5438C>G
NG_013087.1:g.607G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.127+75C>G MANE Select ENSP00000222214.4:n.127+75C>G
ENST00000222214.9:c.127+75C>G ENSP00000222214.4:n.127+75C>G
ENST00000421816.6:n.168+202C>G
ENST00000585420.5:n.259C>G
ENST00000585760.5:n.163+75C>G
ENST00000587072.1:c.127+75C>G ENSP00000468584.1:n.127+75C>G
ENST00000587832.5:n.184+75C>G
ENST00000588905.5:c.91+202C>G ENSP00000465770.1:n.91+202C>G
ENST00000589039.5:c.127+75C>G ENSP00000465618.1:n.127+75C>G
ENST00000590445.5:c.202C>G ENSP00000468125.1:p.Gln68Glu
ENST00000590530.5:c.127+75C>G ENSP00000468452.1:n.127+75C>G
ENST00000590627.5:n.259C>G
ENST00000591043.1:n.163+75C>G
ENST00000591470.5:c.127+75C>G ENSP00000466845.1:n.127+75C>G
NM_000159.3:c.127+75C>G NP_000150.1:n.127+75C>G
NM_013976.3:c.127+75C>G NP_039663.1:n.127+75C>G
NR_102316.1:n.235+75C>G
NR_102317.1:n.310C>G
XM_006722721.2:c.127+75C>G XP_006722784.1:n.127+75C>G
XM_011527899.1:c.127+75C>G XP_011526201.1:n.127+75C>G
XM_011527900.1:c.127+75C>G XP_011526202.1:n.127+75C>G
XM_011527899.2:c.127+75C>G XP_011526201.1:n.127+75C>G
XM_011527900.2:c.127+75C>G XP_011526202.1:n.127+75C>G
XM_017026580.1:c.127+75C>G XP_016882069.1:n.127+75C>G
NM_000159.4:c.127+75C>G MANE Select NP_000150.1:n.127+75C>G
NM_013976.4:c.127+75C>G NP_039663.1:n.127+75C>G
NM_013976.5:c.127+75C>G NP_039663.1:n.127+75C>G