Canonical Allele Identifier: CA2167970
Gene: CHRND HGNC NCBI

Linked Data

dbSNP Id: rs774721327

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232528238G>C , CM000664.2:g.232528238G>C GRCh38
NC_000002.11:g.233392948G>C , CM000664.1:g.233392948G>C GRCh37
NC_000002.10:g.233101192G>C NCBI36
NG_008028.1:g.7027G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258385.8:c.244-24G>C MANE Select ENSP00000258385.3:n.244-24G>C
ENST00000258385.7:c.244-24G>C ENSP00000258385.3:n.244-24G>C
ENST00000412233.5:c.244-24G>C ENSP00000398143.1:n.244-24G>C
ENST00000441621.6:c.244-24G>C ENSP00000408819.2:n.244-24G>C
ENST00000446616.1:c.244-24G>C ENSP00000410801.1:n.244-24G>C
ENST00000449596.5:c.199-24G>C ENSP00000404950.1:n.199-24G>C
ENST00000543200.5:c.199-24G>C ENSP00000438380.1:n.199-24G>C
NM_000751.2:c.244-24G>C NP_000742.1:n.244-24G>C
NM_001256657.1:c.199-24G>C NP_001243586.1:n.199-24G>C
NM_001311195.1:c.-28-24G>C NP_001298124.1:n.-28-24G>C
NM_001311196.1:c.-28-24G>C NP_001298125.1:n.-28-24G>C
NR_046333.1:c.-4294966996-24G>C
NR_046334.1:c.-4294966996-24G>C
XM_011510524.1:c.-28-24G>C XP_011508826.1:n.-28-24G>C
XM_011510524.2:c.-28-24G>C XP_011508826.1:n.-28-24G>C
NM_000751.3:c.244-24G>C MANE Select NP_000742.1:n.244-24G>C
NM_001311195.2:c.-28-24G>C NP_001298124.1:n.-28-24G>C
NM_001311196.2:c.-28-24G>C NP_001298125.1:n.-28-24G>C
NM_001256657.2:c.199-24G>C NP_001243586.1:n.199-24G>C