Canonical Allele Identifier: CA593178950
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs960670476
gnomAD v2: 10-43572482-C-G
gnomAD v3: 10-43077034-C-G
gnomAD v4: 10-43077034-C-G
MyVariant Identifiers: chr10:g.43572482C>G (hg19) chr10:g.43077034C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077034C>G , CM000672.2:g.43077034C>G GRCh38
NC_000010.10:g.43572482C>G , CM000672.1:g.43572482C>G GRCh37
NC_000010.9:g.42892488C>G NCBI36
NG_007489.1:g.4966C>G , LRG_518:g.4966C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-225C>G ENSP00000347942.3:n.-225C>G
XM_011540027.1:c.-225C>G XP_011538329.1:n.-225C>G
NM_020630.5:c.-225C>G NP_065681.1:n.-225C>G
NM_020975.5:c.-225C>G NP_066124.1:n.-225C>G
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