Canonical Allele Identifier: CA2690634714
Gene: ROR2 HGNC NCBI

Linked Data

gnomAD v4: 9-91950000-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91950000T>C , CM000671.2:g.91950000T>C GRCh38
NC_000009.11:g.94712282T>C , CM000671.1:g.94712282T>C GRCh37
NC_000009.10:g.93752103T>C NCBI36
NG_008089.1:g.5163A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.-37A>G MANE Select ENSP00000364860.3:n.-37A>G
ENST00000375708.3:c.-37A>G ENSP00000364860.3:n.-37A>G
NM_004560.3:c.-37A>G NP_004551.2:n.-37A>G
NM_001318204.1:c.-37A>G NP_001305133.1:n.-37A>G
XR_001746315.1:n.207A>G
NM_004560.4:c.-37A>G MANE Select NP_004551.2:n.-37A>G
NM_001318204.2:c.-37A>G NP_001305133.1:n.-37A>G