Canonical Allele Identifier: CA743875981

Gene: PROCR

Linked Data

• dbSNP Id: rs1360427278
• gnomAD v3: 20-35175746-G-T
• gnomAD v4: 20-35175746-G-T
• MyVariant Identifiers: chr20:g.33763549G>T (hg19) ; chr20:g.35175746G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175746G>T , CM000682.2:g.35175746G>T	GRCh38
NC_000020.10:g.33763549G>T , CM000682.1:g.33763549G>T	GRCh37
NC_000020.9:g.33227210G>T	NCBI36
NG_032899.1:g.8776G>T
NG_032899.2:g.8776G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-422G>T MANE Select	ENSP00000216968.3:n.323-422G>T
ENST00000216968.4:c.323-422G>T	ENSP00000216968.3:n.323-422G>T
ENST00000635377.1:c.223-422G>T
NM_006404.4:c.323-422G>T	NP_006395.2:n.323-422G>T
XM_011528496.1:c.323-422G>T	XP_011526798.1:n.323-422G>T
NM_001355008.1:c.-101-9875C>A	NP_001341937.1:n.-101-9875C>A
NM_006404.5:c.323-422G>T MANE Select	NP_006395.2:n.323-422G>T
NM_001355008.2:c.-101-9875C>A	NP_001341937.1:n.-101-9875C>A