Canonical Allele Identifier: CA665362198
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1438754772
gnomAD v3: 10-43077051-C-T
gnomAD v4: 10-43077051-C-T
MyVariant Identifiers: chr10:g.43572499C>T (hg19) chr10:g.43077051C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077051C>T , CM000672.2:g.43077051C>T GRCh38
NC_000010.10:g.43572499C>T , CM000672.1:g.43572499C>T GRCh37
NC_000010.9:g.42892505C>T NCBI36
NG_007489.1:g.4983C>T , LRG_518:g.4983C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-208C>T ENSP00000347942.3:n.-208C>T
XM_011540027.1:c.-208C>T XP_011538329.1:n.-208C>T
NM_020630.5:c.-208C>T NP_065681.1:n.-208C>T
NM_020975.5:c.-208C>T NP_066124.1:n.-208C>T
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