Canonical Allele Identifier: CA658892384

Gene: CWF19L1

Linked Data

• dbSNP Id: rs1249931234
• gnomAD v3: 10-100245729-T-C
• gnomAD v4: 10-100245729-T-C
• MyVariant Identifiers: chr10:g.102005486T>C (hg19) ; chr10:g.100245729T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245729T>C , CM000672.2:g.100245729T>C	GRCh38
NC_000010.10:g.102005486T>C , CM000672.1:g.102005486T>C	GRCh37
NC_000010.9:g.101995476T>C	NCBI36
NG_041811.1:g.26953A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.964+70A>G MANE Select	ENSP00000326411.6:n.964+70A>G
ENST00000354105.8:c.964+70A>G	ENSP00000326411.6:n.964+70A>G
ENST00000370379.1:c.229+70A>G	ENSP00000359405.1:n.229+70A>G
ENST00000466408.1:n.318+70A>G
ENST00000466955.5:n.505+70A>G
ENST00000468709.5:n.820+70A>G
ENST00000478047.1:n.1200-7498A>G
ENST00000482452.5:n.652+70A>G
NM_001303404.1:c.964+70A>G	NP_001290333.1:n.964+70A>G
NM_001303405.1:c.553+70A>G	NP_001290334.1:n.553+70A>G
NM_001303406.1:c.553+70A>G	NP_001290335.1:n.553+70A>G
NM_001303407.1:c.229+70A>G	NP_001290336.1:n.229+70A>G
NM_018294.5:c.964+70A>G	NP_060764.3:n.964+70A>G
NM_018294.6:c.964+70A>G MANE Select	NP_060764.3:n.964+70A>G
NM_001303404.2:c.964+70A>G	NP_001290333.1:n.964+70A>G
NM_001303405.2:c.553+70A>G	NP_001290334.1:n.553+70A>G
NM_001303406.2:c.553+70A>G	NP_001290335.1:n.553+70A>G
NM_001303407.2:c.229+70A>G	NP_001290336.1:n.229+70A>G