Canonical Allele Identifier: CA408710739
Gene: PROCR HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.33764572G>C (hg19) chr20:g.35176769G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176769G>C , CM000682.2:g.35176769G>C GRCh38
NC_000020.10:g.33764572G>C , CM000682.1:g.33764572G>C GRCh37
NC_000020.9:g.33228233G>C NCBI36
NG_032899.1:g.9799G>C
NG_032899.2:g.9799G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216968.5:c.673G>C MANE Select ENSP00000216968.3:p.Val225Leu
ENST00000216968.4:c.673G>C ENSP00000216968.3:p.Val225Leu
ENST00000634509.1:c.94+323G>C ENSP00000489456.1:n.94+323G>C
ENST00000635377.1:c.502-318G>C
NM_006404.4:c.673G>C NP_006395.2:p.Val225Leu
XM_011528496.1:c.601+323G>C XP_011526798.1:n.601+323G>C
NM_001355008.1:c.-101-10898C>G NP_001341937.1:n.-101-10898C>G
NM_006404.5:c.673G>C MANE Select NP_006395.2:p.Val225Leu
NM_001355008.2:c.-101-10898C>G NP_001341937.1:n.-101-10898C>G
Search 100 bp 5'
Search 100 bp 3'