Canonical Allele Identifier: CA351005829

Gene: CHRND

Linked Data

• dbSNP Id: rs1362920655
• gnomAD v2: 2-233399037-G-C
• MyVariant Identifiers: chr2:g.233399037G>C (hg19) ; chr2:g.232534327G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534327G>C , CM000664.2:g.232534327G>C	GRCh38
NC_000002.11:g.233399037G>C , CM000664.1:g.233399037G>C	GRCh37
NC_000002.10:g.233107281G>C	NCBI36
NG_008028.1:g.13116G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1356G>C MANE Select	ENSP00000258385.3:p.Gln452His
ENST00000258385.7:c.1356G>C	ENSP00000258385.3:p.Gln452His
ENST00000441621.6:c.*538G>C	ENSP00000408819.2:n.*538G>C
ENST00000446616.1:c.*997G>C	ENSP00000410801.1:n.*997G>C
ENST00000543200.5:c.1311G>C	ENSP00000438380.1:p.Gln437His
NM_000751.2:c.1356G>C	NP_000742.1:p.Gln452His
NM_001256657.1:c.1311G>C	NP_001243586.1:p.Gln437His
NM_001311195.1:c.774G>C	NP_001298124.1:p.Gln258His
NM_001311196.1:c.1053G>C	NP_001298125.1:p.Gln351His
NR_046333.1:c.-4294966195G>C
NR_046334.1:c.-4294965916G>C
XM_011510524.1:c.975G>C	XP_011508826.1:p.Gln325His
XM_011510524.2:c.975G>C	XP_011508826.1:p.Gln325His
NM_000751.3:c.1356G>C MANE Select	NP_000742.1:p.Gln452His
NM_001311195.2:c.774G>C	NP_001298124.1:p.Gln258His
NM_001311196.2:c.1053G>C	NP_001298125.1:p.Gln351His
NM_001256657.2:c.1311G>C	NP_001243586.1:p.Gln437His