Canonical Allele Identifier: CA2608894058
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43077053-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077053G>C , CM000672.2:g.43077053G>C GRCh38
NC_000010.10:g.43572501G>C , CM000672.1:g.43572501G>C GRCh37
NC_000010.9:g.42892507G>C NCBI36
NG_007489.1:g.4985G>C , LRG_518:g.4985G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-206G>C ENSP00000347942.3:n.-206G>C
XM_011540027.1:c.-206G>C XP_011538329.1:n.-206G>C
NM_020630.5:c.-206G>C NP_065681.1:n.-206G>C
NM_020975.5:c.-206G>C NP_066124.1:n.-206G>C
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