Canonical Allele Identifier: CA313480805

Gene: PROCR

Linked Data

• dbSNP Id: rs1053639490
• gnomAD v2: 20-33763784-C-G
• gnomAD v3: 20-35175981-C-G
• gnomAD v4: 20-35175981-C-G
• MyVariant Identifiers: chr20:g.33763784C>G (hg19) ; chr20:g.35175981C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175981C>G , CM000682.2:g.35175981C>G	GRCh38
NC_000020.10:g.33763784C>G , CM000682.1:g.33763784C>G	GRCh37
NC_000020.9:g.33227445C>G	NCBI36
NG_032899.1:g.9011C>G
NG_032899.2:g.9011C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-187C>G MANE Select	ENSP00000216968.3:n.323-187C>G
ENST00000216968.4:c.323-187C>G	ENSP00000216968.3:n.323-187C>G
ENST00000635377.1:c.223-187C>G
NM_006404.4:c.323-187C>G	NP_006395.2:n.323-187C>G
XM_011528496.1:c.323-187C>G	XP_011526798.1:n.323-187C>G
NM_001355008.1:c.-101-10110G>C	NP_001341937.1:n.-101-10110G>C
NM_006404.5:c.323-187C>G MANE Select	NP_006395.2:n.323-187C>G
NM_001355008.2:c.-101-10110G>C	NP_001341937.1:n.-101-10110G>C