Canonical Allele Identifier: CA306260619

Gene: CRLF1

Linked Data

• dbSNP Id: rs1010586021
• gnomAD v3: 19-18597013-C-G
• gnomAD v4: 19-18597013-C-G
• MyVariant Identifiers: chr19:g.18707823C>G (hg19) ; chr19:g.18597013C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18597013C>G , CM000681.2:g.18597013C>G	GRCh38
NC_000019.9:g.18707823C>G , CM000681.1:g.18707823C>G	GRCh37
NC_000019.8:g.18568823C>G	NCBI36
NG_013370.1:g.14838G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.734G>C	ENSP00000506849.1:p.Arg245Pro
ENST00000392386.8:c.734G>C MANE Select	ENSP00000376188.2:p.Arg245Pro
ENST00000392386.7:c.734G>C	ENSP00000376188.2:p.Arg245Pro
ENST00000597131.1:c.199G>C
NM_004750.4:c.734G>C	NP_004741.1:p.Arg245Pro
XM_011528422.1:c.668G>C	XP_011526724.1:p.Arg223Pro
XM_011528423.1:c.734G>C	XP_011526725.1:p.Arg245Pro
XM_011528424.1:c.668G>C	XP_011526726.1:p.Arg223Pro
XM_011528422.2:c.668G>C	XP_011526724.1:p.Arg223Pro
XM_011528423.2:c.734G>C	XP_011526725.1:p.Arg245Pro
XM_011528424.3:c.668G>C	XP_011526726.1:p.Arg223Pro
NM_004750.5:c.734G>C MANE Select	NP_004741.1:p.Arg245Pro