Canonical Allele Identifier: CA2608894064
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43077057-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077057T>G , CM000672.2:g.43077057T>G GRCh38
NC_000010.10:g.43572505T>G , CM000672.1:g.43572505T>G GRCh37
NC_000010.9:g.42892511T>G NCBI36
NG_007489.1:g.4989T>G , LRG_518:g.4989T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-202T>G ENSP00000347942.3:n.-202T>G
XM_011540027.1:c.-202T>G XP_011538329.1:n.-202T>G
NM_020630.5:c.-202T>G NP_065681.1:n.-202T>G
NM_020975.5:c.-202T>G NP_066124.1:n.-202T>G
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