Canonical Allele Identifier: CA313480737

Gene: PROCR

Linked Data

• dbSNP Id: rs548878861
• gnomAD v3: 20-35175865-G-A
• gnomAD v4: 20-35175865-G-A
• MyVariant Identifiers: chr20:g.33763668G>A (hg19) ; chr20:g.35175865G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175865G>A , CM000682.2:g.35175865G>A	GRCh38
NC_000020.10:g.33763668G>A , CM000682.1:g.33763668G>A	GRCh37
NC_000020.9:g.33227329G>A	NCBI36
NG_032899.1:g.8895G>A
NG_032899.2:g.8895G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216968.5:c.323-303G>A MANE Select	ENSP00000216968.3:n.323-303G>A
ENST00000216968.4:c.323-303G>A	ENSP00000216968.3:n.323-303G>A
ENST00000635377.1:c.223-303G>A
NM_006404.4:c.323-303G>A	NP_006395.2:n.323-303G>A
XM_011528496.1:c.323-303G>A	XP_011526798.1:n.323-303G>A
NM_001355008.1:c.-101-9994C>T	NP_001341937.1:n.-101-9994C>T
NM_006404.5:c.323-303G>A MANE Select	NP_006395.2:n.323-303G>A
NM_001355008.2:c.-101-9994C>T	NP_001341937.1:n.-101-9994C>T