Canonical Allele Identifier: CA206710300
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs373375997
gnomAD v3: 10-43077037-T-A
gnomAD v4: 10-43077037-T-A
MyVariant Identifiers: chr10:g.43572485T>A (hg19) chr10:g.43077037T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077037T>A , CM000672.2:g.43077037T>A GRCh38
NC_000010.10:g.43572485T>A , CM000672.1:g.43572485T>A GRCh37
NC_000010.9:g.42892491T>A NCBI36
NG_007489.1:g.4969T>A , LRG_518:g.4969T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-222T>A ENSP00000347942.3:n.-222T>A
XM_011540027.1:c.-222T>A XP_011538329.1:n.-222T>A
NM_020630.5:c.-222T>A NP_065681.1:n.-222T>A
NM_020975.5:c.-222T>A NP_066124.1:n.-222T>A
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