Canonical Allele Identifier: CA632626060

Gene: CRLF1

Linked Data

• dbSNP Id: rs753694843
• gnomAD v2: 19-18707622-A-G
• gnomAD v3: 19-18596812-A-G
• gnomAD v4: 19-18596812-A-G
• MyVariant Identifiers: chr19:g.18707622A>G (hg19) ; chr19:g.18596812A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596812A>G , CM000681.2:g.18596812A>G	GRCh38
NC_000019.9:g.18707622A>G , CM000681.1:g.18707622A>G	GRCh37
NC_000019.8:g.18568622A>G	NCBI36
NG_013370.1:g.15039T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684169.1:c.856-22T>C	ENSP00000506849.1:n.856-22T>C
ENST00000392386.8:c.856-22T>C MANE Select	ENSP00000376188.2:n.856-22T>C
ENST00000392386.7:c.856-22T>C	ENSP00000376188.2:n.856-22T>C
ENST00000597131.1:c.321-22T>C
NM_004750.4:c.856-22T>C	NP_004741.1:n.856-22T>C
XM_011528422.1:c.790-22T>C	XP_011526724.1:n.790-22T>C
XM_011528423.1:c.856-22T>C	XP_011526725.1:n.856-22T>C
XM_011528424.1:c.790-22T>C	XP_011526726.1:n.790-22T>C
XM_011528422.2:c.790-22T>C	XP_011526724.1:n.790-22T>C
XM_011528423.2:c.856-22T>C	XP_011526725.1:n.856-22T>C
XM_011528424.3:c.790-22T>C	XP_011526726.1:n.790-22T>C
NM_004750.5:c.856-22T>C MANE Select	NP_004741.1:n.856-22T>C