Canonical Allele Identifier: CA1905813974
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1588848261
gnomAD v4: 10-43077040-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077040T>C , CM000672.2:g.43077040T>C GRCh38
NC_000010.10:g.43572488T>C , CM000672.1:g.43572488T>C GRCh37
NC_000010.9:g.42892494T>C NCBI36
NG_007489.1:g.4972T>C , LRG_518:g.4972T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-219T>C ENSP00000347942.3:n.-219T>C
XM_011540027.1:c.-219T>C XP_011538329.1:n.-219T>C
NM_020630.5:c.-219T>C NP_065681.1:n.-219T>C
NM_020975.5:c.-219T>C NP_066124.1:n.-219T>C
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