Canonical Allele Identifier: CA2361537816

Gene: PROCR

Linked Data

• dbSNP Id: rs1600734637
• gnomAD v3: 20-35175970-T-C
• gnomAD v4: 20-35175970-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175970T>C , CM000682.2:g.35175970T>C	GRCh38
NC_000020.10:g.33763773T>C , CM000682.1:g.33763773T>C	GRCh37
NC_000020.9:g.33227434T>C	NCBI36
NG_032899.1:g.9000T>C
NG_032899.2:g.9000T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-198T>C MANE Select	ENSP00000216968.3:n.323-198T>C
ENST00000216968.4:c.323-198T>C	ENSP00000216968.3:n.323-198T>C
ENST00000635377.1:c.223-198T>C
NM_006404.4:c.323-198T>C	NP_006395.2:n.323-198T>C
XM_011528496.1:c.323-198T>C	XP_011526798.1:n.323-198T>C
NM_001355008.1:c.-101-10099A>G	NP_001341937.1:n.-101-10099A>G
NM_006404.5:c.323-198T>C MANE Select	NP_006395.2:n.323-198T>C
NM_001355008.2:c.-101-10099A>G	NP_001341937.1:n.-101-10099A>G