Canonical Allele Identifier: CA783936414

Gene: CRLF1

Linked Data

• dbSNP Id: rs1371157594
• gnomAD v4: 19-18599890-T-C
• MyVariant Identifiers: chr19:g.18710700T>C (hg19) ; chr19:g.18599890T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599890T>C , CM000681.2:g.18599890T>C	GRCh38
NC_000019.9:g.18710700T>C , CM000681.1:g.18710700T>C	GRCh37
NC_000019.8:g.18571700T>C	NCBI36
NG_013370.1:g.11961A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.116-44A>G	ENSP00000506849.1:n.116-44A>G
ENST00000392386.8:c.116-44A>G MANE Select	ENSP00000376188.2:n.116-44A>G
ENST00000392386.7:c.116-44A>G	ENSP00000376188.2:n.116-44A>G
ENST00000593286.1:n.368-44A>G
NM_004750.4:c.116-44A>G	NP_004741.1:n.116-44A>G
XM_011528422.1:c.50-44A>G	XP_011526724.1:n.50-44A>G
XM_011528423.1:c.116-44A>G	XP_011526725.1:n.116-44A>G
XM_011528424.1:c.50-44A>G	XP_011526726.1:n.50-44A>G
XM_011528422.2:c.50-44A>G	XP_011526724.1:n.50-44A>G
XM_011528423.2:c.116-44A>G	XP_011526725.1:n.116-44A>G
XM_011528424.3:c.50-44A>G	XP_011526726.1:n.50-44A>G
NM_004750.5:c.116-44A>G MANE Select	NP_004741.1:n.116-44A>G