Canonical Allele Identifier: CA2608894059
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43077054-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077054C>A , CM000672.2:g.43077054C>A GRCh38
NC_000010.10:g.43572502C>A , CM000672.1:g.43572502C>A GRCh37
NC_000010.9:g.42892508C>A NCBI36
NG_007489.1:g.4986C>A , LRG_518:g.4986C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-205C>A ENSP00000347942.3:n.-205C>A
XM_011540027.1:c.-205C>A XP_011538329.1:n.-205C>A
NM_020630.5:c.-205C>A NP_065681.1:n.-205C>A
NM_020975.5:c.-205C>A NP_066124.1:n.-205C>A
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