Canonical Allele Identifier: CA10654457

Gene: RET

Linked Data

• ClinVar Variation Id: 368899
• ClinVar RCV Id: RCV000295854 ; RCV000317662 ; RCV000350719 ; RCV000372338 ; RCV000836537
• dbSNP Id: rs10900297
• gnomAD v2: 10-43572511-C-A
• gnomAD v3: 10-43077063-C-A
• gnomAD v4: 10-43077063-C-A
• MyVariant Identifiers: chr10:g.43572511C>A (hg19) ; chr10:g.43077063C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077063C>A , CM000672.2:g.43077063C>A	GRCh38
NC_000010.10:g.43572511C>A , CM000672.1:g.43572511C>A	GRCh37
NC_000010.9:g.42892517C>A	NCBI36
NG_007489.1:g.4995C>A , LRG_518:g.4995C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355710.7:c.-196C>A	ENSP00000347942.3:n.-196C>A
XM_011540027.1:c.-196C>A	XP_011538329.1:n.-196C>A
NM_020630.5:c.-196C>A	NP_065681.1:n.-196C>A
NM_020975.5:c.-196C>A	NP_066124.1:n.-196C>A