Canonical Allele Identifier: CA119913
Gene: CSRP3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 8778
dbSNP Id: rs104894205

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188286A>G , CM000673.2:g.19188286A>G GRCh38
NC_000011.9:g.19209833A>G , CM000673.1:g.19209833A>G GRCh37
NC_000011.8:g.19166409A>G NCBI36
NG_011932.2:g.27288T>C , LRG_440:g.27288T>C

Transcript Alleles

HGVS Amino-acid change
NM_003476.4:c.131T>C VV NP_003467.1:p.Leu44Pro
XM_024448698.1:c.113-1938T>C XP_024304466.1:p.=
ENST00000265968.7:c.131T>C ENSP00000265968.3:p.Leu44Pro
ENST00000533783.1:c.131T>C ENSP00000431813.1:p.Leu44Pro