Canonical Allele Identifier: CA10654456

Gene: RET

Linked Data

• ClinVar Variation Id: 368898
• ClinVar RCV Id: RCV000265906 ; RCV000281211 ; RCV000320981 ; RCV000375701 ; RCV001692084
• dbSNP Id: rs10900296
• gnomAD v2: 10-43572507-A-G
• gnomAD v3: 10-43077059-A-G
• gnomAD v4: 10-43077059-A-G
• MyVariant Identifiers: chr10:g.43572507A>G (hg19) ; chr10:g.43077059A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077059A>G , CM000672.2:g.43077059A>G	GRCh38
NC_000010.10:g.43572507A>G , CM000672.1:g.43572507A>G	GRCh37
NC_000010.9:g.42892513A>G	NCBI36
NG_007489.1:g.4991A>G , LRG_518:g.4991A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355710.7:c.-200A>G	ENSP00000347942.3:n.-200A>G
XM_011540027.1:c.-200A>G	XP_011538329.1:n.-200A>G
NM_020630.5:c.-200A>G	NP_065681.1:n.-200A>G
NM_020975.5:c.-200A>G	NP_066124.1:n.-200A>G