Canonical Allele Identifier: CA743876961

Gene: PROCR

Linked Data

• dbSNP Id: rs896629674
• MyVariant Identifiers: chr20:g.33764488G>C (hg19) ; chr20:g.35176685G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176685G>C , CM000682.2:g.35176685G>C	GRCh38
NC_000020.10:g.33764488G>C , CM000682.1:g.33764488G>C	GRCh37
NC_000020.9:g.33228149G>C	NCBI36
NG_032899.1:g.9715G>C
NG_032899.2:g.9715G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.602-13G>C MANE Select	ENSP00000216968.3:n.602-13G>C
ENST00000216968.4:c.602-13G>C	ENSP00000216968.3:n.602-13G>C
ENST00000634509.1:c.94+239G>C	ENSP00000489456.1:n.94+239G>C
ENST00000635377.1:c.501+239G>C
NM_006404.4:c.602-13G>C	NP_006395.2:n.602-13G>C
XM_011528496.1:c.601+239G>C	XP_011526798.1:n.601+239G>C
NM_001355008.1:c.-101-10814C>G	NP_001341937.1:n.-101-10814C>G
NM_006404.5:c.602-13G>C MANE Select	NP_006395.2:n.602-13G>C
NM_001355008.2:c.-101-10814C>G	NP_001341937.1:n.-101-10814C>G