Canonical Allele Identifier: CA2379656660

Gene: CHODL

Linked Data

• dbSNP Id: rs2055011

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18109036G>T , CM000683.2:g.18109036G>T	GRCh38
NC_000021.8:g.19481354G>T , CM000683.1:g.19481354G>T	GRCh37
NC_000021.7:g.18403225G>T	NCBI36
NG_029478.1:g.196698G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000400127.5:c.-45+81065G>T	ENSP00000382992.1:n.-45+81065G>T
ENST00000400128.5:c.-44-147473G>T	ENSP00000382993.1:n.-44-147473G>T
ENST00000400131.5:c.-44-147473G>T	ENSP00000382996.1:n.-44-147473G>T
ENST00000400135.5:c.-45+81065G>T	ENSP00000383001.1:n.-45+81065G>T
NM_001204175.1:c.-44-147473G>T	NP_001191104.1:n.-44-147473G>T
NM_001204176.1:c.-45+81065G>T	NP_001191105.1:n.-45+81065G>T
NM_001204177.1:c.-44-147473G>T	NP_001191106.1:n.-44-147473G>T
NM_001204178.1:c.-45+81065G>T	NP_001191107.1:n.-45+81065G>T
XM_011529455.1:c.-44-147473G>T	XP_011527757.1:n.-44-147473G>T
XM_011529456.1:c.-45+81065G>T	XP_011527758.1:n.-45+81065G>T
XM_011529457.1:c.-44-147473G>T	XP_011527759.1:n.-44-147473G>T
XM_011529457.2:c.-44-147473G>T	XP_011527759.1:n.-44-147473G>T
NM_001204175.2:c.-44-147473G>T	NP_001191104.1:n.-44-147473G>T
NM_001204176.2:c.-45+81065G>T	NP_001191105.1:n.-45+81065G>T
NM_001204177.2:c.-44-147473G>T	NP_001191106.1:n.-44-147473G>T
NM_001204178.2:c.-45+81065G>T	NP_001191107.1:n.-45+81065G>T