Canonical Allele Identifier: CA506044626

Gene: CRLF1

Linked Data

• dbSNP Id: rs1183671538
• gnomAD v2: 19-18710481-A-C
• gnomAD v4: 19-18599671-A-C
• MyVariant Identifiers: chr19:g.18710481A>C (hg19) ; chr19:g.18599671A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599671A>C , CM000681.2:g.18599671A>C	GRCh38
NC_000019.9:g.18710481A>C , CM000681.1:g.18710481A>C	GRCh37
NC_000019.8:g.18571481A>C	NCBI36
NG_013370.1:g.12180T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.291T>G	ENSP00000506849.1:p.Ala97=
ENST00000392386.8:c.291T>G MANE Select	ENSP00000376188.2:p.Ala97=
ENST00000392386.7:c.291T>G	ENSP00000376188.2:p.Ala97=
NM_004750.4:c.291T>G	NP_004741.1:p.Ala97=
XM_011528422.1:c.225T>G	XP_011526724.1:p.Ala75=
XM_011528423.1:c.291T>G	XP_011526725.1:p.Ala97=
XM_011528424.1:c.225T>G	XP_011526726.1:p.Ala75=
XM_011528422.2:c.225T>G	XP_011526724.1:p.Ala75=
XM_011528423.2:c.291T>G	XP_011526725.1:p.Ala97=
XM_011528424.3:c.225T>G	XP_011526726.1:p.Ala75=
NM_004750.5:c.291T>G MANE Select	NP_004741.1:p.Ala97=