Canonical Allele Identifier: CA665362218
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1191017949
gnomAD v4: 10-43077057-T-C
MyVariant Identifiers: chr10:g.43572505T>C (hg19) chr10:g.43077057T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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