Canonical Allele Identifier: CA9314088

Gene: CRLF1

Linked Data

• dbSNP Id: rs750546273
• ExAC: 19:18707696 G / A
• gnomAD v2: 19-18707696-G-A
• gnomAD v4: 19-18596886-G-A
• MyVariant Identifiers: chr19:g.18707696G>A (hg19) ; chr19:g.18596886G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596886G>A , CM000681.2:g.18596886G>A	GRCh38
NC_000019.9:g.18707696G>A , CM000681.1:g.18707696G>A	GRCh37
NC_000019.8:g.18568696G>A	NCBI36
NG_013370.1:g.14965C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.855+6C>T	ENSP00000506849.1:n.855+6C>T
ENST00000392386.8:c.855+6C>T MANE Select	ENSP00000376188.2:n.855+6C>T
ENST00000392386.7:c.855+6C>T	ENSP00000376188.2:n.855+6C>T
ENST00000597131.1:c.320+6C>T
NM_004750.4:c.855+6C>T	NP_004741.1:n.855+6C>T
XM_011528422.1:c.789+6C>T	XP_011526724.1:n.789+6C>T
XM_011528423.1:c.855+6C>T	XP_011526725.1:n.855+6C>T
XM_011528424.1:c.789+6C>T	XP_011526726.1:n.789+6C>T
XM_011528422.2:c.789+6C>T	XP_011526724.1:n.789+6C>T
XM_011528423.2:c.855+6C>T	XP_011526725.1:n.855+6C>T
XM_011528424.3:c.789+6C>T	XP_011526726.1:n.789+6C>T
NM_004750.5:c.855+6C>T MANE Select	NP_004741.1:n.855+6C>T