Canonical Allele Identifier: CA595466947

Gene: CWF19L1

Linked Data

• dbSNP Id: rs1244732795
• gnomAD v2: 10-102005682-A-G
• gnomAD v4: 10-100245925-A-G
• MyVariant Identifiers: chr10:g.102005682A>G (hg19) ; chr10:g.100245925A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245925A>G , CM000672.2:g.100245925A>G	GRCh38
NC_000010.10:g.102005682A>G , CM000672.1:g.102005682A>G	GRCh37
NC_000010.9:g.101995672A>G	NCBI36
NG_041811.1:g.26757T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.850-12T>C MANE Select	ENSP00000326411.6:n.850-12T>C
ENST00000354105.8:c.850-12T>C	ENSP00000326411.6:n.850-12T>C
ENST00000370379.1:c.115-12T>C	ENSP00000359405.1:n.115-12T>C
ENST00000466408.1:n.192T>C
ENST00000466955.5:n.391-12T>C
ENST00000468709.5:n.706-12T>C
ENST00000478047.1:n.1199+7496T>C
ENST00000482452.5:n.538-12T>C
ENST00000496796.5:n.614-12T>C
NM_001303404.1:c.850-12T>C	NP_001290333.1:n.850-12T>C
NM_001303405.1:c.439-12T>C	NP_001290334.1:n.439-12T>C
NM_001303406.1:c.439-12T>C	NP_001290335.1:n.439-12T>C
NM_001303407.1:c.115-12T>C	NP_001290336.1:n.115-12T>C
NM_018294.5:c.850-12T>C	NP_060764.3:n.850-12T>C
NM_018294.6:c.850-12T>C MANE Select	NP_060764.3:n.850-12T>C
NM_001303404.2:c.850-12T>C	NP_001290333.1:n.850-12T>C
NM_001303405.2:c.439-12T>C	NP_001290334.1:n.439-12T>C
NM_001303406.2:c.439-12T>C	NP_001290335.1:n.439-12T>C
NM_001303407.2:c.115-12T>C	NP_001290336.1:n.115-12T>C