Canonical Allele Identifier: CA2608894001
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43077031-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077031A>T , CM000672.2:g.43077031A>T GRCh38
NC_000010.10:g.43572479A>T , CM000672.1:g.43572479A>T GRCh37
NC_000010.9:g.42892485A>T NCBI36
NG_007489.1:g.4963A>T , LRG_518:g.4963A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-228A>T ENSP00000347942.3:n.-228A>T
XM_011540027.1:c.-228A>T XP_011538329.1:n.-228A>T
NM_020630.5:c.-228A>T NP_065681.1:n.-228A>T
NM_020975.5:c.-228A>T NP_066124.1:n.-228A>T
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