Canonical Allele Identifier: CA2608894069
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43077062-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077062T>G , CM000672.2:g.43077062T>G GRCh38
NC_000010.10:g.43572510T>G , CM000672.1:g.43572510T>G GRCh37
NC_000010.9:g.42892516T>G NCBI36
NG_007489.1:g.4994T>G , LRG_518:g.4994T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-197T>G ENSP00000347942.3:n.-197T>G
XM_011540027.1:c.-197T>G XP_011538329.1:n.-197T>G
NM_020630.5:c.-197T>G NP_065681.1:n.-197T>G
NM_020975.5:c.-197T>G NP_066124.1:n.-197T>G
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