Canonical Allele Identifier: CA994214026

Gene: CRLF1

Linked Data

• dbSNP Id: rs1976136258
• gnomAD v3: 19-18596596-T-C
• gnomAD v4: 19-18596596-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596596T>C , CM000681.2:g.18596596T>C	GRCh38
NC_000019.9:g.18707406T>C , CM000681.1:g.18707406T>C	GRCh37
NC_000019.8:g.18568406T>C	NCBI36
NG_013370.1:g.15255A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+26A>G	ENSP00000506849.1:n.1024+26A>G
ENST00000392386.8:c.1024+26A>G MANE Select	ENSP00000376188.2:n.1024+26A>G
ENST00000392386.7:c.1024+26A>G	ENSP00000376188.2:n.1024+26A>G
ENST00000597131.1:c.447+68A>G
NM_004750.4:c.1024+26A>G	NP_004741.1:n.1024+26A>G
XM_011528422.1:c.958+26A>G	XP_011526724.1:n.958+26A>G
XM_011528423.1:c.1024+26A>G	XP_011526725.1:n.1024+26A>G
XM_011528424.1:c.958+26A>G	XP_011526726.1:n.958+26A>G
XM_011528422.2:c.958+26A>G	XP_011526724.1:n.958+26A>G
XM_011528423.2:c.1024+26A>G	XP_011526725.1:n.1024+26A>G
XM_011528424.3:c.958+26A>G	XP_011526726.1:n.958+26A>G
NM_004750.5:c.1024+26A>G MANE Select	NP_004741.1:n.1024+26A>G